Cyclic sulfonamide herbicides

ABSTRACT

Compounds of Formula I and II, and their agriculturally-suitable salts, are disclosed which are useful for controlling undesired vegetation ##STR1## wherein X is a direct bond; O; S; NH; N(C 1  -C 3  alkyl); N(C 1  -C 3  haloalkyl); or N(allyl); 
     R 1  is H; F; Cl; or Br; 
     R 2  is H; F; Cl; Br; CF 3  ; nitro; or cyano; 
     R 4  is H; C 1  -C 3  alkyl; or halogen; 
     R 5  is H; C 1  -C 6  alkyl; C 1  -C 6  haloalkyl; halogen; S(O) 2  (C 1  -C 6  alkyl); or C(═O)R 8  ; or 
     R 4  and R 5  are taken together along with the carbon to which they are attached to form a spiro-cyclopropane ring; 
     and R 3 , R 8 , and J are as defined in the disclosure. 
     Also disclosed are compositions containing the compounds of Formulae I and II and a method for controlling undesired vegetation which involves contacting the vegetation or its environment with an effective amount of a compound of Formula I or II.

This is a division of application Ser. No. 08/737,649 filed Nov. 13, 1996, now U.S. Pat. No. 5,750,471.

BACKGROUND OF THE INVENTION

This invention relates to certain cyclic sulfonamides, their agriculturally-suitable salts and compositions, and methods of their use as general or selective preemergent or postemergent herbicides.

New compounds effective for controlling the growth of undesired vegetation are in constant demand. In the most common situation, such compounds are sought to selectively control the growth of weeds in useful crops such as cotton, rice, corn, wheat, citrus and soybeans, to name a few. Unchecked weed growth in such crops (including plantation crops) can cause significant losses, reducing profit to the farmer and increasing costs to the consumer. In other situations, herbicides are desired which will control all plant growth. Examples of areas in which complete control of all vegetation is desired are areas around railroad tracks, storage tanks and industrial storage areas. There are many products commercially available for these purposes, but the search continues for products which are more effective, less costly and environmentally safe.

U.S. Pat. No. 4,818,275 discloses herbicidal acyclic sulfonamides of the formula ##STR2## wherein, inter alia X and Y are Br; Cl; or F;

R is alkyl; haloalkyl; or dialkylamino; and

R¹ is H; Na; lower alkyl; or SO₂ R.

JP 63 1988!-222167 discloses herbicidal cyclic amides and sulfonamides of the formula ##STR3## wherein X is H or halogen;

Z is O or S;

J is, inter alia, --CO-- or --SO₂₋₋ ;

L₁ is --CO-- or --CR₄ (R₅)--;

R₄ and R₅ are each independently, inter alia, H, C₁ -C₆ alkyl, C₁ -C₆ haloalkyl, or CO₂ R_(a) ;

R₁ is, inter alia, H, C₂ -C₆ alkoxyalkyl, C₁ -C₆ alkyl, C₁ -C₆ haloalkyl, C₂ -C₆ alkenyl, C₂ -C₆ haloalkenyl, C₃ -C₈ cycloalkyl, --COR_(b), --CO₂ R_(b), or --CH₂ CO₂ R_(b) ;

W is, inter alia, ##STR4## Q is N or CH; E is O or S;

R₁₂ is H, C₁ -C₆ alkyl, or C₁ -C₆ haloalkyl when Q is N; or

R₁₂ is H, C₁ -C₆ alkyl, C₁ -C₆ haloalkyl, or C₄ alkylene which combines with Q to form a 6-membered ring when Q is CH;

R₁₃ is H, C₁ -C₆ alkyl, or C₁ -C₆ haloalkyl when Q is N; or

R₁₃ is H, C₁ -C₆ alkyl, C₁ -C₆ haloalkyl, or C₄ alkylene which combines with Q to form a 6-membered ring when Q is CH; and

m is 0 or 1.

The cyclic sulfonamides of the present invention are not disclosed in either of these references.

SUMMARY OF THE INVENTION

This invention includes compounds of Formulae I and II including all geometric and stereoisomers, agriculturally suitable salts thereof, agricultural compositions containing them and their use for controlling undesirable vegetation: ##STR5## wherein X is a direct bond; O; S; NH; N(C₁ -C₃ alkyl); N(C₁ -C₃ haloalkyl); or N(allyl);

R¹ is H; F; Cl; or Br;

R² is H; F; Cl; Br; CF₃ ; nitro; or cyano;

R³ is H; C₁ -C₈ alkyl; C₃ -C₈ cycloalkyl; C₃ -C₈ alkenyl; C₃ -C₈ alkynyl; C₁ -C₈ haloalkyl; C₂ -C₈ alkoxyalkyl; C₃ -C₈ alkoxyalkoxyalkyl; C₃ -C₈ haloalkynyl; C₃ -C₈ haloalkenyl; C₁ -C₈ alkylsulfonyl; C₁ -C₈ haloalkylsulfonyl; C₃ -C₈ alkoxycarbonylalkyl; S(O)₂ NH(C₁ -C₈ alkyl); C(O)R⁶ ; or benzyl optionally substituted on the phenyl ring with R⁷ ;

R⁴ is H; C₁ -C₃ alkyl; or halogen;

R⁵ is H; C₁ -C₆ alkyl; C₁ -C₆ haloalkyl; halogen; S(O)₂ (C₁ -C₆ alkyl); or C(═O)R⁸ ; or

R⁴ and R⁵ are taken together along with the carbon to which they are attached to form a spiro-cyclopropane ring;

R⁶ is C₁ -C₆ alkyl; C₁ -C₆ haloalkyl; C₁ -C₆ alkoxy; NH(C₁ -C₆ alkyl); phenyl optionally substituted with R⁷ ; benzyl; or C₂ -C₈ dialkylamnino;

R⁷ is C₁ -C₆ alkyl; 1-2 halogen; C₁ -C₆ alkoxy; or CF₃ ;

R⁸ is H; C₁ -C₆ alkyl; C₁ -C₆ alkoxy; or NH(C₁ -C₆ alkyl);

J is ##STR6## wherein the dashed line in J-5, J-6 and J-12 indicates that the left-hand ring contains only single bonds or one bond in the ring is a carbon-carbon double bond;

n and m are each independently 0; 1; 2; or 3; provided that m+n is 2 or 3;

Z is CR⁹ R¹⁰ ; O; S; S(O); S(O)₂ ; N(C₁ -C₄ alkyl; or ##STR7## each R⁹ is independently H; C₁ -C₃ alkyl; halogen; hydroxy; C₁ -C₆ alkoxy; C₁ -C₆ haloalkyl; C₁ -C₆ haloalkoxy; C₂ -C₆ alkylcarbonyloxy; or C₂ -C₆ haloalkylcarbonyloxy;

each R¹⁰ is independently H; C₁ -C₃ alkyl; hydroxy; or halogen;

R¹¹ and R¹² are each independently H; halogen; C₁ -C₆ alkyl; C₃ -C₆ alkenyl; or C₁ -C₆ haloalkyl;

R¹³ is H; C₁ -C₆ alkyl; C₁ -C₆ haloalkyl; C₃ -C₆ alkenyl; C₃ -C₆ haloalkenyl; C₃ -C₆ alkynyl; C₃ -C₆ haloalkynyl; HC(═O); (C₁ -C₄ alkyl)C(═O); or NH₂ ;

R¹⁴ is C₁ -C₆ alkyl; C₁ -C₆ alkylthio; C₁ -C₆ haloalkyl; CF₃ ; or N(CH₃)₂ ;

W is N or CR¹⁵ ;

R¹⁵ is H; C₁ -C₆ alkyl; halogen; or phenyl optionally substituted with C₁ -C₆ alkyl, 1-2 halogen, C₁ -C₆ alkoxy, or CF₃ ;

each Q is independently O or S;

Q¹ is O or S;

Z¹ is CR¹⁶ R¹⁷ ; O; S; S(O); S(O)₂ ; N(C₁ -C₄ alkyl; or ##STR8## each R¹⁶ is independently H; halogen; hydroxy; C₁ -C₆ alkoxy; C₁ -C₆ haloalkyl; C₁ -C₆ haloalkoxy; C₂ -C₆ alkylcarbonyloxy; or C₂ -C₆ haloalkylcarbonyloxy;

each R¹⁷ is independently H; hydroxy; or halogen; or

when R¹⁶ and R¹⁷ are bonded to adjacent atoms they can be taken together with the carbons to which they are attached to form ##STR9## R¹⁸ is C₁ -C₆ alkyl; halogen; or C₁ -C₆ haloalkyl;

R¹⁹ and R²⁰ are each independently H; C₁ -C₆ alkyl; or C₁ -C₆ haloalkyl;

R²¹ and R²² are each independently C₁ -C₆ alkyl; C₁ -C₆ haloalkyl; C₃ -C₆ alkenyl; C₃ -C₆ haloalkenyl; C₃ -C₆ alkynyl; or C₃ -C₆ haloalkynyl;

R²³ is halogen or cyano;

R²⁴ is C₁ -C₆ alkylsulfonyl; C₁ -C₆ alkyl; C₁ -C₆ haloalkyl; C₃ -C₆ alkenyl; C₃ -C₆ alkynyl; C₁ -C₆ alkoxy; C₁ -C₆ haloalkoxy; or halogen;

R²⁵ is C₁ -C₆ alkyl; C₁ -C₆ haloalkyl; C₃ -C₆ alkenyl; or C₃ -C₆ alkynyl; and

R²⁶ is C₁ -C₆ alkyl; C₁ -C₆ haloalkyl; or phenyl optionally substituted with C₁ -C₆ alkyl, 1-2 halogen, 1-2 nitro, C₁ -C₆ alkoxy, or CF₃ ;

provided that when X is O or S in Formula II, then J is other than J-6 or J-7.

In the above recitations, the term "alkyl", used either alone or in compound words such as "alkylthio" or "haloalkyl" includes straight-chain or branched alkyl, such as, methyl, ethyl, n-propyl, i-propyl, or the different butyl, pentyl or hexyl isomers. "Alkenyl" includes straight-chain or branched alkenes such as 1-propenyl, 2-propenyl, and the different butenyl, pentenyl and hexenyl isomers. "Alkenyl" also includes polyenes such as 1,3-hexadienyl and 2,4,6-heptatrienyl. "Alkynyl" includes straight-chain or branched alkynes such as 1-propynyl, 3-propynyl and the different butynyl, pentynyl and hexynyl isomers. "Alkynyl" can also include moieties comprised of multiple triple bonds such as 2,7-octadiynyl. "Alkoxy" includes, for example, methoxy, ethoxy, n-propyloxy, isopropyloxy and the different butoxy, pentoxy and hexyloxy isomers. "Alkoxyalkyl" denotes alkoxy substitution on alkyl. "Alkoxyalkoxy" denotes alkoxy substitution on alkoxy. Examples of "alkoxyalkyl" include CH₃ OCH₂, CH₃ OCH₂ CH₂, CH₃ CH₂ OCH₂, CH₃ CH₂ CH₂ CH₂ OCH₂ and CH₃ CH₂ OCH₂ CH₂. "Alkylthio" includes branched or straight-chain alkylthio moieties such as methylthio, ethylthio, and the different propylthio, butylthio, pentylthio and hexylthio isomers. Examples of "alkylsulfonyl" include CH₃ S(O)₂, CH₃ CH₂ S(O)₂, CH₃ CH₂ CH₂ S(O)₂, (CH₃)₂ CHS(O)₂ and the different butylsulfonyl, pentylsulfonyl and hexylsulfonyl isomers. "Dialkylamino" is defined analogously to the above examples. "Cycloalkyl" includes, for example, cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl.

The term "halogen", either alone or in compound words such as "haloalkyl", includes fluorine, chlorine, bromine or iodine. The term "1-2 halogen" indicates that one or two of the available positions for that substituent may be halogen. Further, when used in compound words such as "haloalkyl", said alkyl may be partially or fully substituted with halogen atoms which may be the same or different. Examples of "haloalkyl" include F₃ C, ClCH₂, CF₃ CH₂ and CF₃ CCl₂. The terms "haloalkenyl", "haloalkynyl" "haloalkoxy", and the like are defined analogously to the term "haloalkyl". Examples of "haloalkenyl" include (Cl)₂ C═CHCH₂ and CF₃ CH₂ CH═CHCH₂. Examples of "haloalkynyl" include HC.tbd.CCHCl, CF₃ C.tbd.C, CCl₃ C.tbd.C and FCH₂ C.tbd.CCH₂. Examples of "haloalkoxy" include CF₃ O, CCl₃ CH₂ O, HCF₂ CH₂ CH₂ O and CF₃ CH₂ O. Examples of "haloalkylsulfonyl" include CF₃ SO₂, CCl₃ SO₂, CF₃ CH₂ SO₂ and CF₃ CF₂ SO₂.

The total number of carbon atoms in a substituent group is indicated by the "C_(i) -C_(j) " prefix where i and j are numbers from 1 to 8. For example, C₁ -C₃ alkylsulfonyl designates methylsulfonyl through propylsulfonyl; C₂ alkoxyalkoxy designates CH₃ OCH₂ O; C₃ alkoxyalkoxy designates, for example, CH₃ CH(OCH₃)O, CH₃ OCH₂ CH₂ O or CH₃ CH₂ OCH₂ O; and C₄ alkoxyalkoxy designates the various isomers of an alkoxy group substituted with a second alkoxy group containing a total of four carbon atoms, examples including CH₃ CH₂ CH₂ OCH₂ O, and CH₃ CH₂ OCH₂ CH₂ O. Examples of "alkylcarbonyl" include C(O)CH₃, C(O)CH₂ CH₂ CH₃ and C(O)CH(CH₃)₂. Examples of "alkoxycarbonyl" include CH₃ OC(═O), CH₃ CH₂ OC(═O), CH₃ CH₂ CH₂ OC(═O), (CH₃)₂ CHOC(═O) and the different butoxy-, pentoxy- or hexyloxycarbonyl isomers.

When a group contains a substituent which can be hydrogen, for example R¹ or R⁹, then, when this substituent is taken as hydrogen, it is recognized that this is equivalent to said group being unsubstituted by that substituent.

Compounds of this invention can exist as one or more stereoisomers. The various stereoisomers include enantiomers, diastereomers, atropisomers and geometric isomers. One skilled in the art will appreciate that one stereoisomer may be more active and/or may exhibit beneficial effects when enriched relative to the other stereoisomer(s) or when separated from the other stereoisomer(s). Additionally, the skilled artisan knows how to separate and/or to selectively prepare said stereoisomers. Accordingly, the present invention comprises mixtures, individual stereoisomers, and optically active mixtures of compounds of Formulae I and II as well as agriculturally suitable salts thereof.

The salts of the compounds of the invention include acid-addition salts with inorganic or organic acids such as hydrobromic, hydrochloric, nitric, phosphoric, sulfuric, acetic, butyric, fumaric, lactic, maleic, malonic, oxalic, propionic, salicylic, tartaric, 4-toluenesulfonic or valeric acids. The salts of the compounds of the invention also include those formed with organic bases (e.g., pyridine, ammonia, or triethylamine) or inorganic bases (e.g., hydrides, hydroxides, or carbonates of sodium, potassium, lithium, calcium, magnesium or barium) when the compound contains an acidic group.

Preferred compounds, compositions containing them, and methods of their use for reasons of better activity and/or ease of synthesis are:

Preferred 1. Compounds of Formulae I and II above, and agriculturally-suitable salts thereof, wherein:

X is a direct bond or O;

R¹ is F or Cl;

R² is F; Cl; or Br;

R³ is H; C₁ -C₆ alkyl; C₃ -C₆ cycloalkyl; C₃ -C₆ alkenyl; C₃ -C₆ alkynyl; C₁ -C₆ haloalkyl; C₂ -C₆ alkoxyalkyl; C₃ -C₆ haloalkenyl; C₁ -C₆ alkylsufonyl; C₃ -C₆ alkoxycarbonylalkyl; C(O)R⁶ ; or benzyl optionally substituted on the phenyl ring with R⁷ ;

R⁴ is H or halogen;

R⁵ is H;

J is J-1; J-2; J-3; J-4; J-5; J-6; J-8; J-12; J-15; or J-16;

Z is CR⁹ R¹⁰ ; O; S; or N(C₁ -C₄ alkyl);

each R⁹ is independently H; halogen; or C₁ -C₆ haloalkoxy;

each R¹⁰ is independently H or halogen;

each Q is O;

Q¹ is S;

Z¹ is CR¹⁶ R¹⁷ ; O; S; or N(C₁ -C₄ alkyl);

each R¹⁶ is independently H; halogen; or haloalkoxy;

each R¹⁷ is independently H or halogen; or

when R¹⁶ and R¹⁷ are bonded to adjacent atoms they can be taken together with the carbons to which they are attached to form ##STR10## R¹⁸ is t-butyl or CH₂ CH₂ CH₂ F; R²³ is Cl or cyano; and

R²⁴ is C₁ -C₄ haloalkyl or C₁ -C₆ haloalkoxy.

Preferred 2. Compounds of Preferred 1 wherein:

R² is F or Cl;

R³ is C₁ -C₆ alkyl; C₃ -C₆ cycloalkyl; C₃ -C₆ alkenyl; C₃ -C₆ alkynyl; C₃ -C₆ alkoxycarbonylalkyl; or benzyl optionally substituted on the phenyl ring with R⁷ ;

J is J-1; J-2; J-3; J-4; J-5; J-6; J-8; or J-12;

Z is CR⁹ R¹⁰ or O;

each R⁹ is independently H or halogen;

R¹¹ is C₁ -C₄ haloalkyl;

R¹² is C₁ -C₄ alkyl;

R¹³ is CH₃ ;

R¹⁴ is CF₃ ;

W is CH;

Z¹ is CR¹⁶ R¹⁷ or O;

each R¹⁶ is independently H or halogen;

each R¹⁷ is independently H or halogen; or

when R¹⁶ and R¹⁷ are bonded to adjacent atoms they can be taken together with the carbons to which they are attached to form ##STR11## Preferred 3. Compounds of Preferred 2 wherein: R² is Cl;

R³ is C₁ -C₆ alkyl; C₃ -C₆ alkenyl; or C₃ -C₆ alkynyl;

J is J-1; J-2; J-3; J-4; J-6; or J-12;

Z is CR⁹ R¹⁰ ;

R⁹ is independently H or F;

R¹⁰ is independently H or F;

R¹¹ is CF₂ H;

R¹² is CH₃ ;

Z¹ is CR¹⁶ R¹⁷ ;

R¹⁶ is independently H or F; and

R¹⁷ is independently H or F.

Most preferred are compounds of Preferred 1 selected from the group:

3- 7-chloro-5-fluoro-1,3-dihydro-1 - (4-methoxyphenyl)methyl!-2,1-benzisothiazol-4-yl!-1-methyl-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedione S,S-dioxide;

3-(7-chloro-5-fluoro-1,3-dihydro-2,1 -benzisothiazol-4-yl)-1-methyl-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedione S,S-dioxide;

3-(7-chloro-1-ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-yl)-1-methyl-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedione S,S-dioxide; and

3- (7-chloro-1-ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-yl)imino!tetrahydro-1H,3H- 1,3,4!thiadiazolo 3,4-α!pyridazin-1-one S,S-dioxide.

The invention further comprises anilines of Formula 1 and 2 wherein R¹, R², R³, R⁴, R⁵ and X are as defined for compounds of Formula I and II above. The anilines are intermediates in the preparation of compounds of Formula I and II. ##STR12##

DETAILS OF THE INVENTION

The compounds of Formulae I and II can be prepared by one or more of the following methods, or variations obvious to one skilled in the art, as described below in Schemes 1-21. The definitions of Z, Z¹, Q, Q¹, X, W, n, m, and R¹ through R²⁶ in the compounds of Formulae 1-46 below are as defined above in the Summary of the Invention. Compounds of Formulae Ia-Ir are various subsets of the compounds of Formula I, and all substituents for Formulae Ia-Ir are as defined above for Formula I.

Compounds of Formulae I and II are prepared from the corresponding anilines of Formulae 1 and 2, respectively, as represented in Scheme 1. ##STR13## Synthesis of Anilines of Formulae 1 and 2

Anilines of Formulae 1 and 2 wherein X is a direct bond (Formula 2a) are prepared by the method illustrated in Scheme 2. The nitro aniline of Formula 3 is treated with a sulfonyl chloride in the presence of a base such as pyridine, N,N-dimethylaminopyridine (DMAP), or triethylamine at -20° to 25° C. to obtain the sulfonamide of Formula 4. For compounds wherein R³ is other than H, the sulfonamide nitrogen can be alkylated or acylated to give the R³ -substituted compound of Formula 5. The alkylation is performed using an alkyl halide or alkyl sulfonate in the presence of a base such as potassium carbonate, sodium methoxide, potassium t-butoxide (t-BuOK), or sodium hydride in an anhydrous solvent such as dimethylformamide (DMF), tetrahydrofaran, or acetonitrile at ambient temperature to 80° C. Acylations to form the R³ ═C(O)R⁶ compounds are accomplished by condensing the sulfonamide of Formula 4 with the appropriate acylating agent, for example an acyl chloride, isocyanate or carbamoyl chloride. ##STR14##

The cyclization to form the cyclic sulfonamide functionality is achieved via intramolecular vicarious nucleophilic substitution of hydrogen as described by K. Wojciechowski and M. Makosza in Synthesis, (1992), 571. Treatment of the sulfonamide of Formula 5 with a base such as sodium hydroxide, sodium methoxide, or potassium t-butoxide in an inert solvent such as dimethyl sulfoxide (Me₂ SO), dimethylformamide or tetrahydrofuran at a temperature between -60° C. and ambient temperature affords the cyclic sulfonamides of Formulae 6 and 7. The ratio of products depends on the nature of R², and the base and solvent used in the cyclization. If R² is other than hydrogen, only compounds of Formula 6 are obtained. When R² is hydrogen and a mixture of products is obtained, the isomers can be separated by chromatography or crystallization techniques.

The nitro group in the compounds of Formulae 6 and 7 can be reduced to the corresponding anilines of Formula 1 and 2a, respectively, using iron-HCl, SnCl2.H₂ O, or hydrogen over palladium on carbon.

In some instances, it may be desirable to introduce a non-hydrogen R² group in anilines of Formula 1 after cyclization. For example, introduction of a chlorine or bromine atom to give anilines of Formula 1a can be accomplished using N-chlorosuccinimide (NCS) or N-bromosuccinimide (NBS), respectively, in an inert solvent such as dimethylformamide (DMF) at a temperature between ambient temperature and 80° C.

The nitro compounds of Formula 3 are prepared as illustrated in Scheme 3. The amino group of the aniline of Formula 8 is protected with a suitable protecting group, for example as the phthalimide by reaction with phthalic anhydride, to give the protected aniline of Formula 9. For suitable amino protecting groups, see T. W. Greene and P. G. M. Wuts, Protective Groups in Organic Synthesis, 2nd Edition, John Wiley and Sons, Inc., New York, (1991).

Nitration of 9 using a nitric acid/sulfric acid mixture at -20° to 20° C. affords the nitro compound of Formula 10. Deprotection of the amino group (using hydrazine in the case of the phthalimide group) affords the nitroaniline of Formula 3. ##STR15##

The anilines of Formula 8 are known or can be prepared by well-known methods (see March, J., Advanced Organic Chemistry, (1992), 4th Ed., John Wiley and Sons, Inc., pp 591, 1103-1105).

Anilines of Formulae 1 and 2a can also be prepared by introduction of the nitro group further along in the synthetic pathway as illustrated in Scheme 4. ##STR16##

The aniline of Formula 8 is contacted with a sulfonyl chloride as described above to give the sulfonamide of Formula 11. N-Acylation with an acyl chloride or the like, or N-alkylation with an R³ -halide or -sulfonate in the presence of a base, as described above provides the N-substituted sulfonamide of Formula 12. Nitration to form the nitro compound of Formula 13 can be achieved using a nitric acid/sulfuric acid mixture at -20° to 20° C. Vicarious intramolecular nucleophilic substitution followed by reduction of the nitro group using the conditions described previously affords the anilines of Formulae 1 and 2a.

Anilines of Formula 2 wherein X is other than a direct bond (Formula 2b) can be prepared starting from the corresponding amino phenol (X═O), amino thiophenol (X═S), or diamine (X═NH or N(C₁ -C₃ alkyl)) of Formula 14 as illustrated in Scheme 5. Using conditions described above, the aniline is treated with a sulfonyl chloride to give the sulfonamide of Formula 15. Subsequent treatment with a base, for example potassium carbonate, induces cyclization. Nitration with nitric and sulfuric acid affords the corresponding nitro compound of Formula 16. N-Alkylation or N-acylation to introduce R³ followed by reduction of the nitro group using the reaction conditions described above gives the aniline of Formula 2b. ##STR17##

A similar but alternative method for the preparation of anilines of Formula 2b is outlined in Scheme 6. Starting with the nitro compound of Formula 17, the phenol (X═O), thiol (X═S), or amino (X═NH or N(C₁ -C₃ alkyl)) group is protected with a suitable protecting group (see T. W. Greene and P. G. M. Wuts, Protective Groups in Organic Synthesis, 2nd Edition, John Wiley and Sons, Inc., New York, (1991)). For example, a benzyl (Bn) group is a particularly suitable protecting group and is introduced by treatment with benzyl bromide (BnBr) in the presence of K₂ CO₃. Reduction of the nitro group, for example with iron and HCl as described above, affords the aniline of Formula 18. Condensation with a sulfonyl chloride followed by N-alkylation or N-acylation affords the N-substituted sulfonamide of Formula 19. ##STR18##

Removal of the protecting group under the appropriate conditions (for example, by treatment with hydrogen over palladium on carbon in the case of an OBn group) and treatment with base induces cyclization to form the cyclic sulfonamide. Nitration and reduction as described above affords the aniline of Formula 2b.

Converting Anilines of Formulae 1 and 2 to Compounds of Formulae I and II

The anilines prepared by the methods outlined in Schemes 1-6 are used in the condensation with J group derivatives to form compounds of Formulae I and II. In some instances, the anilines are used directly in the condensation reactions. In other instances and depending on the nature of the J-group, the NH₂ of the aniline is first converted to another functional group prior to condensation. For example, the aniline may be converted first to a hydrazine, an isocyanate or an aryl iodide. These methods are described in more detail below.

Direct Coupling with the Anilines

In some instances where the aniline is used directly, the compounds of Formulae I and II are prepared by condensation of the aniline with an anhydride precursor to the J group. For example, as illustrated in Scheme 7, the anhydride of Formula 20 is condensed with the aniline of Formula 1 to give compounds of Formula Ia wherein J=J-1. This method is disclosed in EP-A-170,191. ##STR19##

The anhydride of Formula 20 can be prepared by methods disclosed in EP 493,721, and WO 91/06216. Compounds of Formulae I and II wherein J=J-11 and J-18 can be prepared using similar methodology. The aniline is condensed with the appropriate J-group anhydride, diester, or other bis-electrophile to form the compound of Formula I or II. The synthesis of the J-11 precursor and the condensation reaction is described in EP 454,444 and EP 415,642. The J-18 group anhydride and the aniline condensation reaction are described in U.S. Pat. No. 4,003,926.

The sulfonamides of Formulae I and II wherein J=J-10 are also prepared directly from the anilines of Formula 1 and 2, respectively. The J-10 group precursor and the aniline condensation reaction are described in WO 94/03459.

Hydrazines

For some compounds of Formulae I and II, the appropriate aniline is first converted to the corresponding hydrazine, and then the hydrazine is condensed with the J-group derivative, or precursor thereof, to form the desired material. The conversion of an aniline of Formula 1 to a hydrazine of Formula 21 is illustrated in Scheme 8. Subsequent condensation of the hydrazine with the iminoether precursor to J-2 followed by cyclization with phosgene forms the cyclic sulfonamide of Formula Ib. The preparation of the iminoether J-2 precursor and the condensation procedure is described in U.S. Pat. No. 4,315,767. ##STR20##

Anilines can be converted to the hydrazines by diazotization and then reduction as is well-known in the literature (for example, see U.S. Pat. No. 4,695,312).

Compounds of Formulae I and II wherein J=J-3 and J-8 are also prepared by first converting the aniline to the appropriate hydrazine, and then condensation with the appropriate J-group precursor. Methods for the preparation of the J-3 precursor and the condensation are described in U.S. Pat. No. 5,215,958, WO 90/02120, and U.S. Pat. No. 4,818,275. Methods for the preparation of the J-8 precursor and the condensation with a hydrazine are described in WO 92/12139 and U.S. Pat. No. 4,560,752.

For some compounds of Formulae I and II wherein J=J-2 and Z is CR⁹ R¹⁰, the synthesis is carried out as illustrated below in Schemes 9-17. The retrosynthetic analysis for the synthesis of the J-2 group is shown below (Scheme 9). The formation of ring A can be accomplished by intramolecular cyclization between the nitrogen in ring B and the terminal double bond of the triazolinone with the cyclic sulfonamide group already in place. ##STR21##

The synthesis of the triazolinone ring B is known in the art and can be prepared by methods such as those described in U.S. Pat. No. 4,818,275 and U.S. Pat. No. 4,818,276. Acidic condensation of α-ketoacids of Formula 22 and a substituted phenyl hydrazine such as that of Formula 23 gives hydrazones of Formula 24. This reaction is performed under acidic conditions using hydrochloric acid in an organic solvent such as ethyl or methyl alcohol at a temperature between room temperature and about 100° C. Schmidt rearrangement of the acid of Formula 24 with diphenylphosphoryl azide between about 0° C. and about 100° C. followed by a ring cyclization gives the triazolinones as shown below (Scheme 10). The same conditions can be used to form the precursors to compounds of Formula II except the substituted phenyl hydrazine would contain the other cyclic sulfonamide functionality. ##STR22##

For the synthesis of the triazolinones wherein R¹⁰ is H, 2-oxo-5-hexenoic acid of Formula 22a can be used as the starting material. 2-Oxo-5-hexenoic acid can be made by hydrolysis of the corresponding methyl ester with base, preferably one equivalent of potassium hydroxide in an aqueous alcohol solvent. The ester of 2-oxo-5-hexenoic acid is made from methyl pyruvate as described in J Org. Chem., (1983), 48, 158.

Treatment of the triazolinone with MCPBA (m-chloroperoxybenzoic acid) in an inert solvent such as dichloromethane at a temperature between about 0° C. and about 100° C., preferably at room temperature, gives an epoxide of Formula 25 (Scheme 11). Intramolecular cyclization of the epoxide using a base such as potassium carbonate in an inert solvent such as acetonitrile or acetone gives the 6-membered ring product of Formula Ic. Fluorination of the alcohol of Formula Ic with DAST (diethylaminosulfur trifluoride) at a temperature between about -78° C. and about 100° C. in an inert solvent such as dichloromethane gives the fluorinated product of Formula Id. ##STR23##

The alcohol of Formula Ic can also be prepared by hydroxybromination of the olefin in the starting triazolinone using N-bromosuccinimide (NBS) and water or N-bromoacetamide and water followed by cyclization of the resulting bromohydrin of Formula 26 using potassium carbonate in an inert solvent such as acetonitrile or acetone (Scheme 12). ##STR24##

Compounds of Formula Ic can also be converted to the chloro-, bromo-, and iodo-R⁹ substituted triazolinones of Formula I wherein J=J-2 using methods known to those skilled in the art. For example, the hydroxy group in compounds of Formula Ic can be acylated by known methods to prepare the alkylcarbonyloxy and haloalkylcarbonyloxy derivatives. In addition, the hydroxy or halo group can be converted by known methods to afford the R⁹ =alkoxy and haloalkoxy derivatives (March, J., Advanced Organic Chemistry, (1992), 4th Ed., John Wiley and Sons, Inc., pp 386-389). In fact all the R⁹ =OH or halogen compounds in Schemes 13-17 can be functionalized as is known in the art to prepare the other R⁹ substituted compounds.

Compounds of Formulae Ie and If can be prepared as illustrated in Scheme 13. Oxidative cleavage of the olefin of the triazolinone using sodium periodate and a catalytic amount of osmium tetroxide in an inert solvent mixture such as tetrahydrofuran (THF) and water, or using ozone in dichloromethane followed by reductive workup using dimethyl sulfide (DMS), affords the aldehyde of Formula 27. Intramolecular cyclization of the aldehyde under basic conditions using potassium carbonate or sodium hydride gives the 5-membered ring alcohol of Formula Ie. Treatment of the alcohol of Formula Ie with DAST in an inert solvent such as dichloromethane at a temperature between about -80° C. and about 60° C. produces the fluoride of Formula If. The fluoride If can also be made by direct cyclization and fluorination using DAST at a temperature range between about -100° C. and about 60° C. ##STR25##

Hydroboration of the olefin of the triazolinone with 9-borabicyclo 3.3.1!nonane (9-BBN) gives the alcohol of Formula 28 after oxidative workup (Scheme 14). Oxidation of alcohol 28 with oxidizing agents such as PDC (pyridinium dichromate) produces the hemiaminal of Formula Ig presumably via the aldehyde intermediate of Formula 29. The fluoro compound of Formula Ih can be made by the treatment of the hemiaminal with DAST. ##STR26##

Triazolinones of Formula 30 can be made from 2-oxo-4-pentenoic acids and the substituted phenyl hydrazines by methods known to those skilled in the art and the methods taught herein (Scheme 10). The epoxide of Formula 31 can be prepared from the olefin of Formula 30 using an oxidant such as MCPBA. Intramolecular cyclization of the epoxide with a base such as potassium carbonate affords the alcohol of Formula Ii. The fluoro compound of Formula Ij can be made from the alcohol using DAST at a temperature between about -70° C. and about room temperature in an inert solvent such as dichloromethane. ##STR27##

Compounds of Formula Im can be prepared from the unsubstituted compounds of Formula 32 as illustrated in Scheme 16. Treatment of the bicyclic triazolinone of Formula 32 with N-bromosuccinimide (NBS) under allylic bromination conditions affords the mono-bromo derivative of Formula Ik.

Hydrolysis of the bromide in hot aqueous dimethyl sulfoxide (Me₂ SO) affords the alcohol of Formula II. The fluoro compound of Formula Im can be prepared by treatment of the alcohol with diethylaminosulfur trifluoride (DAST) as described above. ##STR28##

Compounds of Formula In can be prepared as illustrated in Scheme 17. Allylic oxidation of the terminal alkene of the triazolinone with t-butyl hydroperoxide and catalytic selenium (IV) oxide in an inert solvent such as dichloromethane produces the allylic alcohol of Formula 33. Protection of the secondary alcohol as the t-butyldimethylsilyl (TBS) ether is accomplished using t-butylchlorodimethylsilane and a base, preferably triethylamine and catalytic 4-(dimethylamino)pyridine. The terminal olefin is converted to the primary alcohol to afford compounds of Formula 34 using 9-BBN followed by treatment with sodium perborate. Ring cyclization is accomplished using the Martin sulflirane dehydrating agent C₆ H₅ (CF₃)₂ O!₂ S(C₆ H₅)₂. Removal of the TBS group and liberation of the alcohol can be accomplished using tetrabutylammonium fluoride. The alcohol can be converted to the corresponding fluoro compound using DAST, or to other R⁹ substituted compounds as described above. ##STR29##

For some compounds of Formulae I and II wherein J=J-2 and R¹⁰ is other than hydrogen, the R¹⁰ substituent is more conveniently introduced after cyclization to form the bicyclic triazolinone. This is especially the case when R⁹ and R¹⁰ are attached to the same carbon atom.

Isocyanates

In some instances, the appropriate aniline is first converted to the corresponding isocyanate, and then the isocyanate is condensed with the J-group derivative, or precursor thereof, to form compounds of Formulae I and II. In Scheme 18, the conversion of aniline of Formula 1 to isocyanate of Formula 35 is illustrated. Subsequent condensation of the isocyanate with the aminoester of Formula 36 forms the cyclic sulfonamide of Formula Io. The preparation of some aminoester precursors to J-6 and the condensation procedure is described in U.S. Pat. No. 4,179,276. ##STR30##

Compounds of Formulae I and II wherein J=J-4, J-5, J-7, J-9, J-11, J-12, J-13, J-14 and J-17 are also prepared by first converting the aniline to the appropriate isocyanate, and then condensation with the appropriate J-group precursor. Methods for the preparation of the J-4 precursor and the condensation are described in WO 92/11244, EP 476,697, ZA 91/00466, JP 77,874, and U.S. Pat. No. 3,902,887. The synthesis of the J-5 precursor and the condensation with isocyanates is described in WO 92/13453 JP 363,278, EP 230,874, and JP 2.000,985. Methods for the preparation of the J-7 precursor and the condensation with isocyanates are described in EP 484,776. Methods for the preparation of the J-9 precursor and the condensation with isocyanates are described in U.S. Pat. No. 5,035,740. Methods for the preparation of the J-17 precursor and its condensation with isocyanates are described in EP 493,323. The synthesis of the J-14 precursor and the condensation with isocyanates is described in J. Pesticide Sci., (1993), 18, 309. In a similar vein, the imino compounds of Formulae I and II wherein J=J-12 and J-13 can be prepared from the corresponding isocyanates of the anilines. The condensation procedure and J-group precursor preparation for compounds containing J-12 and J-13 are disclosed in EP 457,151, JP 4,145,087, EP 480,871 and DE 3,927,388.

One skilled in the art will recognize that when Q or Q¹ is S in the desired product, the appropriate isothiocyanate is used instead of the isocyanate in the synthesis.

For some compounds of Formulae I and II wherein J=J-4, J-5, J-6, J-7, J-9, J-14 and J-17, the coupling can also be accomplished starting with the aniline rather than the isocyanate. For example, the synthesis of compounds of Formula Ip (compounds of Formula I wherein R¹⁶ and R¹⁷ are taken together to form a cyclopropane ring) is illustrated in Scheme 19. ##STR31##

Treatment of cyclopropane dicarboxylic acid of Formula 37 with urea and heating to 175°-185° C. affords the dicarboximide of Formula 38 as described by G. C. Crockett et al. in Synth. Commun. (1981), 11, 447-454. The diester of the diacid of Formula 37 is prepared by the method described by L. L. McCoy in J. Am. Chem. Soc., (1958), 80, 65-68. The diacid can be obtained by saponification of the diester using well-known methods. Reduction of the dicarboximide of Formula 38 with borane in an inert solvent, such as tetrahydrofuran (THF), followed by work-up with aqueous hydrochloric acid affords the azabicyclo 3.1.0!hexane hydrochloride of Formula 39. The reduction is preferably conducted with heating, for example in THF at reflux, as described by H. C. Brown and P. Heim in J. Org. Chem., (1973), 38, 912-916.

The amine hydrochloride of Formula 39 is converted via a five step sequence to the α-aminoacid of Formula 43 as illustrated. Purification of the intermediates is not necessary. Neutralization of the amine hydrochloride with a base, such as concentrated aqueous potassium hydroxide, liberates the free amine. Dissolution of the amine in an inert solvent, such as diethyl ether, and treatment with a solution of N-chlorosuccininide (NCS) in an inert solvent such as ether, produces the chloramine of Formula 40. The solution of the chloramine is then treated with ethanolic potassium hydroxide to effect dehydrochlorination and give the imine of Formula 41. Once again, the imine is not purified but treated directly first with aqueous sodium bisulfite, and then with solid sodium cyanide to afford the arninonitrile of Formula 42. The reaction mixture is poured into water and extracted with a water-immiscible solvent such as ether. The organic layers are dried and evaporated under reduced pressure to afford the aminonitrile. No additional purification is necessary. The aminonitrile can be converted to the aminoacid of Formula 43 by hydrolysis with aqueous barium hydroxide followed by neutralization with sulfuric acid. A mixture of epimers at the carboxylic acid centers is obtained, and the individual diastereomers can be separated by chromatography.

The acid of Formula 43 is reacted with the aniline of Formula and a trialkylaluminum reagent (e.g., trimethylaluminum), in a non-coordinating solvent such as an aromatic hydrocarbon (e.g., benzene and toluene) or halogenated hydrocarbon (e.g., methylene chloride, chloroform, carbon tetrachloride, and dichlorobutane) to obtain the amide. Generally, the reaction requires 0.1 to 48 hours at a temperature of 0° C. to 25° C. to proceed to completion. The amides are isolated by extraction into an organic solvent, aqueous wash, and removal of the solvent under reduced pressure. Purification can be accomplished by chromatography or recrystallization. The condensation with the amine can also be performed starting with the ester of the acid of Formula 43.

The tricyclic imide of Formula Ip can be prepared from the α-arninoamide by condensation with phosgene or a phosgene equivalent. Treatment of the α-aminoamide with phosgene is preferably carried out in the presence of a tertiary-amine base such as triethylamine, pyridine, or N,N-diisopropylethylamine, in an inert solvent such as dichloromethane or 1-chlorobutane. The phosgene can be added as a gas or as a solution in an inert solvent such as toluene. Suitable temperatures range from about 0° C. to the reflux temperature of the solvent. 1,1'-Carbonyldiimidazole, diphosgene (ClC(═O)OCCl₃) and triphosgene (Cl₃ COC(═O)OCCl₃) can also be used in a similar manner.

The tricyclic imide of Formula Ip can be isolated by extraction into an organic solvent, aqueous wash, and removal of the solvent under reduced pressure. Additional purification can be accomplished by chromatography or recrystallization.

Aryl Iodides

For the preparation of compounds of Formulae I and II wherein J=J-15 and J-16, the appropriate aniline is first converted to the aryl alkyne as illustrated in Scheme 20. The aniline of Formula 1 is converted to the aryl iodide of Formula 44 via diazotization followed by treatment with a metal iodide salt. The aryl iodide is linked by a palladium coupling reaction to give the trimethylsilyl (TMS) alkyne. Hydrolysis of the TMS group with base affords the terminal alkyne of Formula 45. In the case of J-16, a 3+2! cycloaddition using a sydnone as the dipole and the alkyne as the dipolarophile affords the bicyclic pyrazole compounds. Introduction of the R²³ group affords the cyclic sulfonamides of Formula Iq. For example, treatment with N-chlorosuccinimide affords the R²³ ═Cl compound. These methods are described in WO 93/15074. ##STR32##

Methods for the similar preparation of compounds of Formulae I and II wherein J=J-15 are described in JP 4,059,706, WO 92/06962, and JP 3,163,063.

For compounds of Formulae I and II wherein J=J-5, the coupling can also be accomplished starting with the aniline rather than the isocyanate. For example, the synthesis of compounds of Formula Ir is illustrated in Scheme 21. Treatment of a diester of Formula 46 with an aniline of Formula 1 in the presence of a trialkylaluminum reagent (e.g., trimethylaluminum) in a non-coordinating solvent such as an aromatic hydrocarbon (e.g., benzene, toluene) or a halogenated hydrocarbon (e.g., methylene chloride, chloroform, carbon tetrachloride and dichlorobutane) affords a compound of Formula Ir. ##STR33##

It is recognized that some reagents and reaction conditions described above for preparing compounds of Formulae I and II may not be compatible with certain functionalities present in the intermediates. In these instances, the incorporation of protection/deprotection sequences or functional group interconversions into the synthesis will aid in obtaining the desired products. The use and choice of the protecting groups will be apparent to one skilled in chemical synthesis (see, for example, Greene, T. W.; Wuts, P. G. M. Protective Groups in Organic Synthesis, 2nd ed.; Wiley: New York, 1991). One skilled in the art will recognize that, in some cases, after the introduction of a given reagent as it is depicted in any individual scheme, it may be necessary to perform additional routine synthetic steps not described in detail to complete the synthesis of compounds of Formulae I and II.

One skilled in the art will also recognize that compounds of Formulae I and II and the intermediates described herein can be subjected to various electrophilic, nucleophilic, radical, organometallic, oxidation, and reduction reactions to add substituents or modify existing substituents.

Without further elaboration, it is believed that one skilled in the art using the preceding description can utilize the present invention to its fullest extent. The following Examples are, therefore, to be construed as merely illustrative, and not limiting of the disclosure in any way whatsoever. Percentages are by weight unless otherwise indicated. Parts for chromatographic solvent mixtures are by volume unless otherwise indicated. ¹ H NMR spectra are reported in ppm downfield from tetramethylsilane; s=singlet, d=doublet, t=triplet, q=quartet, m=multiplet, dd=doublet of doublets, br s=broad singlet.

EXAMPLE 1

Step A

1-Chloro-N-(4-fluoro-3-nitrophenyl)methanesulfonamide

To a solution of 4-fluoro-3-nitroaniline (23.4 g, 0.15 mol) in anhydrous pyridine (120 mL) was added dropwise a solution of chloromethylsulfonyl chloride (22.35 g, 0.15 mol) at 0° C. under a nitrogen atmosphere. The mixture was then stirred at 0°-5° C. for 4 h and then the mixture was poured onto ice (1500 g) containing concentrated aqueous hydrochloric acid (300 mL). The mixture was filtered, and the residue was dissolved in methylene chloride (1200 mL). After drying (MgSO₄) and concentration under reduced pressure, the crude product was dissolved in 1-chlorobutane:ether 9:1 v/v and passed through silica gel. The eluent was concentrated under reduced pressure to give the title compound of Step A.

Step B

1-Chloro-N-ethyl-N-(4-fluoro-3-nitrophenvl)methanesulfonamide

A solution of 1-chloro-N-(4-fluoro-3-nitrophenyl)methanesulfonamide (5.93 g, 22.1 mmol), iodoethane (3.79 g, 24.3 mmol), tetrabutylammonium bromide (0.712 g, 2.21 mmol), and anhydrous K₂ CO₃ (8.85 g, 64 mmol) in anhydrous dimethylformamide (40 mL) was stirred at room temperature. When the starting material had disappeared based on thin layer chromatography on silica (6 h), the reaction mixture was poured into water (200 mL) and extracted with CH₂ Cl₂ (500 mL). The organic extract was washed with water (two times with 50 mL), dried (MgSO₄), and the solvent was removed under reduced pressure. The residue was purified by flash chromatography (silica gel, 1-chlorobutane and diethyl ether 100:1 v/v eluent) to give 4.68 g of the title compound of Step B as a solid melting at 80°-83° C. ¹ H NMR (Me₂ SO-d₆, 400 MHz): δ 8.17 (dd,1H, J=6.75 and 2.7 Hz), 7.85 (dd,1H, J=9.4 and 3 Hz), 7.69 (dd,1H, J=11 and 9 Hz), 5.25 (s,2H), 3.83 (q,2H), 1.04 (t,3H).

Step C

1-Ethyl-5-fluoro-1,3-dihydro-4-nitro-2,1-benzisothiazole2,2-dioxide and 1-Ethyl-6-fluoro-1,3-dihydro-5-nitro-2,1-benzisothiazole 2,2-dioxide

1-Chloro-N-ethyl-N-(4-fluoro-3-nitrophenyl)methanesulfonamide (2.0 g, 6.74 mmol) in dimethyl sulfoxide (Me₂ SO-d₆, 10 mL) was added dropwise to a vigorously stirred suspension of powdered NaOH (4.0 g) in Me₂ SO-d₆ (30 mL) while maintaining the temperature at 25°-27° C. after completion of the addition, the mixture was stirred at 25°-27° C. for an additional 30 min. After completion of the reaction based on thin layer chromatography on silica gel, the reaction mixture was poured into ice (400 g) and concentrated aqueous hydrochloric acid (60 mL). The precipitate was extracted into CH₂ Cl₂ (300 mL), dried (MgSO₄), and subjected to flash chromatography on silica gel using ethyl acetate:hexane 1:4 v/v. Two products were isolated. The first compound to elute was 1-ethyl-6-fluoro-1,3-dihydro-5-nitro-2,1-benzisothiazole 2,2-dioxide (Compound A, 120 mg). The second compound to elute was 1-ethyl-5-fluoro-1,3-dihydro-4-nitro-2,1-benzisothiazole 2,2-dioxide (Compound B, 976 mg). Compound A: ¹ H NMR (CDCl₃, 300 MHz): δ 7.33 (dd,1H, J=10.51 and 9.75 Hz), 6.96 (dd,1H, J=9.0 and 3.38 Hz), 4.63 (s,2H), 3.76 (q,2H), 1.41 (t,3H). Compound B: m.p. 97°-100° C.; ¹ H NMR (CDCl₃, 300 MHz): δ 7.37 (d,1H, J=6.10 Hz), 7.27 (d,1H, J=10.9 Hz), 4.39 (s,2H), 3.74 (q,2H), 1.44 (t,3H).

Step D:

1-Ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-amine 2,2-dioxide

A mixture of 1-ethyl-5-fluoro-1,3-dihydro-4-nitro-2,1-benzisothiazole 2,2-dioxide (1.0 g, 3.8 mmol) and SnCl₂.H₂ O (4.34 g, 19.2 mmol) in ethyl acetate (50 mL) was heated at reflux for 3 h. After completion of the reaction based on thin layer chromatography, the mixture was diluted with ethyl acetate (100 mL) and solid Na₂ CO₃ (12.5 g) was added. The resulting mixture was vigorously stirred for 12 h and then filtered through a pad of diatomaceous earth (Celite®). The filtrate was then evaporated under reduced pressure, and the residue was subjected to flash chromatography (silica gel, chlorobutane:ether 1:10 v/v) to give 650 mg of the title compound of Step D. ¹ H NMR (CDCl₃, 400 MHz): δ 6.94 (m,1H), 6.08 (m,1H), 4.10 (s,2H), 3.80 (br s,2H), 3.62 (q,2H), 1.36 (t,3H).

Step E:

2-(1-Ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazole-4-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione S,S-dioxide

A mixture of 1-ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-amine 2,2-dioxide (506 mg, 2.2 mmol), and 3,4,5,6-tetrahydrophthalic anhydride (335 mg, 2.2 mmol) in acetic acid (10 mL) was heated at reflux for 2 days. Progress of the reaction was monitored by thin layer chromatography. After completion of the reaction, the solvent was removed under reduced pressure and the product was purified by flash chromatography (silica gel, 1-chlorobutane:ether 4:1 v/v) to give 550 mg of the title compound of Step E, a compound of the invention, as a solid melting at 189°-190° C. ¹ H NMR (CDCl₃, 400 MHz): δ 7.18 (dd,1H), 6.72 (dd,1H), 4.20 (s,2H), 3.68 (q,2H), 2.42 (br s,4H), 1.78 (br s,4H), 1.38 (t,3H).

EXAMPLE 2 2-(7-Chloro-1-ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione S,S-dioxide

A mixture of 2-(1-ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazole-4-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione S,S-dioxide (250 mg, 0.686 mmol) and N-chlorosuccinimide (96 mg, 0.72 mmol) in dimethylformamide (3 mL) was heated at 80° C. for 4 h under a nitrogen atmosphere. After completion of the reaction based on thin layer chromatography, the mixture was poured into ether (25 mL) and water (5 mL). The organic phase was separated, dried (MgSO₄) and evaporated under reduced pressure. The residue was then purified by flash chromatography (silica gel, 1-chlorobutane:ether 19:1 v/v as eluent) to give 121 mg of the title compound of Example 2, a compound of the invention, as a solid melting at 190°-192° C. ¹ H NMR (CDCl₃, 400 MHz): δ 7.26 (dd,1H), 4.18 (s,2H), 3.96 (q,2H), 2.45 (m,4H), 1.84 (m,4H), 1.28 (t,3H).

EXAMPLE 3

Step A

1-Ethyl-6-fluoro-1,3-dihydro-2,1-benzisothiazol-5-amine 2,2-dioxide

1-Ethyl-6-fluoro-1,3-dihydro-5-nitro-2,1-benzisothiazole 2,2-dioxide (Compound B from Example 1, Step C, 1.0 g), was suspended in tetrahydrofuran (20 mL) with 10% palladium on carbon (100 mg). The suspension was placed in Parr® shaker and treated with 50 psi (3.45×10⁵ Pa) of hydrogen overnight. The catalyst was then filtered off through diatomaceous earth (Celite®), and the filtrate was evaporated under reduced pressure to give the title compound of Step A as a brown solid (0.510 mg). ¹ H NMR (CDCl₃): δ 6.92 (dd,1H), 6.04 (dd,1H), 4.08 (s,2H), 3.80 (br s,2H), 3.64 (q,2H), 1.32 (t,3H).

Step B

2-(1-Ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazol-6-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione S,S-dioxide

1-Ethyl-6-fluoro-1,3-dihydro-2,1-benzisothiazol-5-amine 2,2-dioxide (123 mg) and 3,4,5,6-tetrahydrophthalic anhydride (64 mg) were condensed using the procedure described in Example 1, Step E to give 64 mg of the title compound of Step B, a compound of the invention. ¹ H NMR (CDCl₃): δ 7.08 (d,1H), 6.62 (d,2H), 4.32 (s,2H), 3.64 (q,2H), 2.42 (m,4H), 1.82 (m,4H), 1.38 (t,3H).

EXAMPLE 4

Step A

7-Chloro-1-ethyl-5-fluoro-1,3-dihydro-4-isocyanato-2,1-benzisothiazole 2,2-dioxide

To a mixture of 7-chloro-1-ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-amine-2,2-dioxide (1.30 g, 4.91 mmol), diphosgene (1.17 g, 1.2 eq) in p-dioxane (20 mL), triethylamine (0.6 g, 1.2 eq) was added and the resulting reaction mixture was heated at reflux for overnight. The precipitated triethylamine hydrochloride was filtered off and the solvents were removed in vacuo and dried to give the title compound of Step A as a brown semisolid. ¹ H NMR (CDCl₃, 400 MHz): δ 7.21 (d,1H, J=9.5 Hz), 4.28 (s,2H), 3.94 (q,2H), 1.22 (t,3H, J=7.5 Hz).

Step B

3-(7-Chloro-1-ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazole-4-yl)-6-(trifluoromethyl)-2.4(1H,3H)-pyrimidinedione S,S-dioxide

A solution of ethyl 3-amino-4,4,4-trifluorocrotonate (0.899 g, 4.91 mmol) in DMF (3 mL) was added to sodium hydride (60% suspension in oil, 0.118 g, 4.91 mmol) in DMF (8.5 mL) at -10 to -5° C. The reaction mixture was stirred at -10 to -5° C. for 30 min and was then cooled to -78° C. To the resulting solution was added a solution of the title compound of Step A in toluene (14 mL). The reaction mixture was stirred for an additional 2 h at -78° C., overnight at room temperature, and was then poured into HCl/ice mixture and extracted with ethyl acetate (20 mL). The organic phase was separated, washed with water (10 mL), dried (MgSO₄), filtered and the solvent was removed on the rotary evaporator. The title compound of Step B, a compound of the invention, was isolated by flash chromatography as a brown solid (1.18 g, m.p. >230° C., R_(f) 0.25 (silica gel) 1:1 1-chlorobutane and ether). ¹ H NMR (Me₂ SO-d₆, 400 MHz): δ 12.92 (broad, 1H, NH), 7.83 (d,1H, 10.0 Hz), 6.46 (s,1H), 4.76 (d,1H, J=16.5 Hz), 4.58 (d,1H, J=16.5 Hz), 3.81 (q,2H), 1.17 (t,3H, J=7.0 Hz).

EXAMPLE 5 3-(7-Chloro-1-ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-yl)-1-methyl-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedione S,S-dioxide

A mixture of the title compound of Step B in Example 4 (0.33 g, 077 mmol), dimethyl sulfate (0.102 g, 1.05 eq) in acetone (10 mL) was heated at reflux in the presence of potassium carbonate (0.213 g) for 3 h. After completion of the reaction (TLC), the reaction mixture was cooled, the insolubles were filtered off and the solvent was removed on a rotary evaporator. The title compound of Example 5, a compound of the invention, was purified by flash chromatography to give a colorless solid melting at 147°-149° C. (R_(f) 0.55, 1:1 1-chlorobutane and ether). ¹ H NMR (benzene-d₆, 400 MHz): δ 6.55 (d,1H, J=9.5 Hz), 5.86 (s,1H), 3.19-3.60 (m,4H), 2.77 (d,1H, J=1.5 Hz), 0.963 (t,3H). IR (KBr) 1636, 1691.

EXAMPLE 6 3-(7-Chloro-1-ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-yl)-1-ethyl-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedione S,S-dioxide

A mixture of the title compound of Step B in Example 4 (0.3 g, 0.70 mmol), ethyl iodide (0.13 g, 0.84 mmol), K₂ CO₃ (0.12 g, 0.88 mmol) in acetone (10 mL) was heated at reflux for 40 h. The reaction mixture was cooled, the insolubles were filtered off, the solvent was removed in vacuo and the title compound of Example 6, a compound of the invention, was purified by flash chromatography to give a solid melting at 177°-178° C. ¹ H NMR: δ 7.24 (d,1H), 6.32 (s,1H), 4.08 (s,2H), 4.04 (m,4H), 1.26 (m,6H).

EXAMPLE 7

Step A

7-Chloro-1-ethyl-5-fluoro-1,3-dihydro-4-isothiocyanato-2,1-benzisothiazole 2,2-dioxide

To a solution of 7-chloro-1-ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-amine 2,2-dioxide (0.5 g, 1.88 mmol) and triethylamine (0.6 mL) in anhydrous tetrahydrofuran (THF, 10 mL), thiophosgene (0.238 g, 1.1 eq) in THF (2 mL) was added dropwise at room temperature under a nitrogen atmosphere. The resulting reaction mixture was heated at reflux for 2 days. The solvents were removed in vacuo to give the title compound of Step A which was used in Step B.

Step B

3- (7-Chloro-1-ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-yl)imino!tetrahydro-1H,3H- 1,3,4!thiadiazolo 3,4-α!pyridazin-1-one S,S-dioxide

A mixture of the title compound of Step A (0.57 g, 1.88 mmol), 1,2,3,6-tetrahydropyridazine (0.675 g, 1.97 mmol) and K₂ CO₃ (1.3 g, 5 eq) in anhydrous THF was stirred at room temperature for 1 h. After completion of the reaction, the solvent was removed and the adduct was purified by flash chromatography. ¹ H NMR (CDCl₃, 300 MHz): δ 9.28 (br s,1H),7.08 (d,1H), 4.21 (s,2H),3.86 (m,3H),3.56 (m,1H), 3.04 (m,2H ), 1.82 (m,4H), 1.26 (t,3H).

To a solution of this adduct (0.342 g, 0.87 mmol) in anhydrous toluene (5 mL) was added a solution of phosgene (0.098 g) in toluene (3 mL) dropwise under a nitrogen atmosphere and the resulting reaction mixture was stirred at room temperature for 12 h. After completion of the reaction (TLC), the solvent was removed under reduced pressure and the title compound of Step B, a compound of the invention, was purified by flash chromatography to give a solid melting at 143°-146° C. ¹ H NMR (CDCl₃, 300 MHz): δ 7.03 (d,1H, 10.8 Hz), 4.16 (s,2H), 3.90 (dd,2H), 3.47 (m,4H), 1.93 (m,4H), 1.20 (t,3H).

EXAMPLE 8 2-(7-Chloro-1-ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-yl)tetrahydroimidazo 1,5α!pyridine-1,3(2H,5H)-dione S,S-dioxide

To a solution of pipecolinic acid (0.205 g, 1.59 mmol) in KOH (93 mg, 1.66 mmol), H₂ O (5 mL) was added the title compound of Step A in Example 4 (0.44 g, 1.5 mmol) in acetone (2.5 mL). The resulting reaction mixture was stirred at room temperature for 20 h. The solvents were then removed and acidified with 3N HCl to pH 1 to obtain a brown precipitate. The mixture was extracted with ethyl acetate (50 mL) and the organic phase was separated. The organic phase was dried (MgSO₄) and the solvent was removed to give a brown solid. This solid was dissolved in ethanol (10 mL) and 3N HCl (10 mL) and heated at reflux for 12 h. The solvents were then removed in vacuo and the residue was extracted with ethyl acetate. The extracts were dried (MgSO₄) and concentrated to give a brown solid. The title compound of Example 8, a compound of the invention, was isolated by flash chromatography using ethyl acetate: hexane (3:7) as eluent giving a solid melting at 168°-169° C. ¹ H NMR (CDCl₃, 400 MHz): δ 7.28 (d,1H, J=9.5 Hz), 4.17-4.36 (m,3H), 3.94 (m,3H), 2.93 (m,1H), 2.32 (m,1H), 2.09 (m,1H), 1.83 (m,1H), 1.40-1.55 (m,3H), 1.28 (t,3H).

EXAMPLE 9 2-(7-Chloro-1-ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-yl)tetrahydro-1H-imidazo- 5,1-c! 1,4!oxazine-1,3(2H)-dione S,S-dioxide

Using similar reaction conditions as described in Example 8, the title compound of Step A in Example 4 (0.44 g, 1.5 mmol) and morpholine carboxylic acid (0.218 g, 1.66 mmol) gave 0.24 g of the title compound of Example 9, a compound of the invention, as a solid melting at 200°-202° C. ¹ H NMR (CDCl₃, 400 MHz): δ 7.27 (d,1H, J=9.5 Hz), 4.36 (m,2H), 4.25 (d,1H), 4.17 (m,1H), 4.03 (m,2H),3.96 (m,2H) , 3.23-3.53 (m,3H), 1.28 (t,3H).

EXAMPLE 10 2-(7-Chloro-1-ethyl-5-fluoro-1,3-dihydro-2,1 -benzisothiazol-4-yl)-5,8-dihydro-1H- 1,2,4!triazolo 1,2-α!pyridazine-1,3(2H)-dione S,S-dioxide

A solution of trimethylaluminum (0.68 mL 2M in hexane, 1.36 mmol) was added dropwise to 7-chloro-1-ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-amine 2,2-dioxide (0.3 g, 1.13 mmol) in toluene (5 mL) at room temperature under a nitrogen atmosphere and the resulting reaction mixture was stirred for 10 min. A solution of diethyl 3,6-dihydro-1,2-pyridazinedicarboxylate (0.313 g, 1.36 mmol) in toluene (2 mL) was then added at room temperature and the reaction mixture was heated at reflux for 12 h. After the reaction was complete, the reaction mixture was poured into a solution of ethyl acetate (40 mL) containing 1N HCl (10 mL) and stirred for 10 min. The organic phase was separated, dried, and the solvent was removed on a rotary evaporator and followed by flash chromatography to afford the title compound of Example 10, a compound of the invention, as a semisolid. ¹ H NMR (CDCl₃, 300 MHz): δ 7.30 (d,1H, J=9.6 Hz), 5.99 (s,2H), 4.31 (s,2H), 4.21 (s,4H), 3.93 (dd,2H), 1.28 (t,3H).

EXAMPLE 11 2-(7-Chloro-1-ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-yl)tetrahvdro-1H- 1,2,4!triazolo 1,2-α!pyridazine-1,3(2H)-dione S,S-dioxide

Using similar reaction conditions as described in Example 10,7-chloro-1-ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-amine 2,2-dioxide (0.46 g, 1.13 mmol) and diethyl hexahydropyridazine-1,2-dicarboxylate (0.314 g, 1.36 mmol) gave the title compound of Example 11, a compound of the invention, as a solid melting at 87°-90° C. ¹ H NMR (CDCl₃,400 MHz):δ7.29 (d,1H), 4.22 (s,2H), 3.95 (q,2H), 3.65 (m,4H), 1.89 (m,4H), 1.28 (t,3H).

EXAMPLE 12

Step A

7-Chloro-1-ethyl-5-fluoro-4-hydrazino-1,3-dihydro-2,1-benzisothiazole 2,2-dioxide

To a suspension of 7-chloro-1-ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-amine 2,2-dioxide (0.5 g, 1.89 mmol) in water (3.1 mL) and H₂ SO₄ (1.65 mL) at 0° C. was added NaNO₂ (0.13 g, 1.89 mmol) in water (0.5 mL). The reaction mixture was stirred at 0° C. for 1 h. A solution of SnCL₂.H₂ O (0.85 g, 3.78 mmol) in conc. HCl (3.1 mL) was then added dropwise and the reaction mixture was stirred at room temperature for 12 h. Then 50% aqueous NaOH solution was added until the reaction mixture reached pH 13. The reaction mixture was extracted with ethyl acetate (200 mL) and the organic layer was washed with brine (3×50 mL) and dried (MgSO₄). The solvent was removed and the title compound of Step A was isolated by flash chromatography. ¹ H NMR (CDCl₃, 300 MHz): δ 7.04 (d,1H), 5.62 (br s,1H), 4.62 (s,2H), 3.86 (m,2H), 1.26 (t,3H).

Step B

A mixture of the title compound of Step A (0.5 g, 1.79 mmol), aqueous HCl (10%, 0.1 mL), ethanol (0.2 mL) and sodium pyruvate (0.21 g, 1.87 mmol) was heated at 40° C. for 1 h. The reaction mixture was then cooled and diluted with water (2 mL) to give a brown solid which was filtered (0.5 g) and used in Step C.

Step C

1-(7-Chloro-1-ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-yl)-2,4-dihydro-5-methyl-3H-1,2,4-triazol-3-one S,S-dioxide

A mixture of the Step B compound (0.78 g, 2.23 mmol), diphenylphosphoryl azide (0.62 g, 2.25 mmol) and triethylamine (0.24 g, 2.32 mmol) in anhydrous toluene (11 mL) was heated at reflux for 5 h. After completion of the reaction (TLC), the reaction mixture was cooled, diluted with ethyl acetate (50 mL) and washed with brine (10 mL). The organic phase was dried (MgSO₄) and the solvent was evaporated. The resulting residue was purified by flash chromatography to give the title compound of Step C as a solid melting at 195°-197° C. ¹ H NMR (Me₂ SO-d₆, 400 MHz): δ 11.92 (br s,1H), 7.79 (d,1H, J=10.25 Hz), 4.71 (s,2H), 3.78 (dd,2H), 2.15 (s,3H), 1.15 (t,3H).

Step D

2-(7-Chloro-1-ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-yl)-4-(difluoromethyl)-2,4-dihydro-5-methyl-3H- 1,2,4-triazol-3-one S,S-dioxide

To a mixture of the title compound of Step C (0.348 g, 1 mmol), tetrabutylammonium bromide (TBAB, 0.25 g), NaOH (0.257 g, 6.43 mmol) in cyclohexane (10 mL) was added Freon® 22 (chlorodifluoromethane, 0.3 mL, 2.98 mmol) and the reaction mixture was heated at 60° C. for 2 h under a Freon® 22 filled balloon. After the reaction was complete, the reaction mixture was cooled and the solvent was removed. The title compound of Step D, a compound of the invention, was isolated by flash chromatography as a semisolid. ¹ H NMR (CDCl₃, 300 MHz): δ 7.32 (d,1H), 7.02 (t,1H), 4.26 (s,2H), 3.96 (q,2H), 2.49 (s,3H), 1.26 (t,3H).

EXAMPLE 13

Step A

1-Chloro-N-(4-fluoro-3-nitrophenyl)-N- (4-methoxphenyl)methyl!methanesulfonamide

A solution of the title compound of Step A in Example 1 (3 g, 11.16 mmol), 4-methoxbenzyl chloride (2.1 g, 13.4 mmol), tetrabutylammonium bromide (0.36 g, 1.1 mmol) and anhydrous K₂ CO₃ (4.5 g, 13.8 mmol) in anhydrous dimethylformamide (20 mL) was stirred at room temperature for 6 h. When the starting material had been consumed based on TLC (silica gel), the reaction mixture was poured into water (100 mL) and extracted with ethyl acetate (250 mL). The organic extract was washed with brine (100 mL), dried (MgSO₄), and the solvent was removed. Flash chromatography of the residue afforded 2.5 g of the title compound of Step A as an oil. ¹ H NMR (CDCl₃, 300 MHz): δ 8.01 (dd,1H, J=6.57 and 2.82 Hz), 7.48 (m,1H), 7.21 (dd,1H, J=10.13, 9.01 Hz), 6.80-7.12 (m,4H), 4.93 (s,2H), 4.57 (s,2H), 3.77 (s,3H).

Step B

5-Fluoro-1,3-dihydro-1- (4-methoxphenyl)methyl!-4-nitro-2,1-benzisothiazole 2,2-dioxide and 5-fluoro-1,3-dihydro-1- (4-methoxphenyl)methyl!-6-nitro-2,1-benzisothiazole 2,2-dioxide

The title compound of Step A (1.66 g, 4.26 mmol) in dimethyl sulfoxide (Me₂ SO, 8 mL) was added dropwise to a vigorously stirred suspension of powdered NaOH (3.32 g) in Me₂ SO (15 mL) while maintaining the temperature at 25°-27° C. After completion of the addition, the reaction mixture was stirred at 25°-27° C. for an additional 45 min. The reaction mixture was then poured into a mixture of ice (600 g) and conc. HCl (40 mL) and extracted with ethyl acetate (300 mL). The organic extract was dried (MgSO₄) and the solvent was removed. Flash chromatography of the resulting residue afforded two products. The first compound to elute was 5-fluoro-1,3-dihydro-1- (4-methoxphenyl)methyl!-6-nitro-2,1-benzisothiazole 2,2-dioxide (Compound A). The second compound to elute was 5-fluoro-1,3-dihydro-1- (4-methoxyphenyl)methyl!-4-nitro-2,1-benzisothiazole 2,2-dioxide (Compound B). Compound A: ¹ H NMR (CDCl₃, 400 MHz): δ 7.26 (m,3H), 6.88 (m,3H), 4.68 (s,2H), 4.46 (s,2H), 3.82 (s,3H). Compound B: ¹ H NMR (CDCl₃, 400 MHz): δ 7.30 (d,2H), 7.16 (t,1H, J=10 Hz), 6.90 (d,2H), 6.74 (dd,1H, J=9.0, 3.5 Hz), 4.73 (d,2H, J=4.5 Hz), 3.80 (s,3H).

Step C

5-Fluoro-1,3-dihydro-1- (4-methoxphenyl)methyl!-2,1-benzisothiazol-4-amine 2,2-dioxide

A mixture of 5-fluoro-1,3-dihydro-1- (4-methoxyphenyl)methyl!-4-nitro-2,1-benzisothiazole 2,2-dioxide (1.54 g, 4.37 mmol) and SnCl₂.H₂ O (4.93 g, 21.9 mmol) in ethyl acetate (200 mL) was heated at reflux for 3 h. Then the reaction mixture was cooled, diluted with ethyl acetate (200 mL) and solid Na₂ CO₃ (15 g) was added. The resulting mixture was vigorously stirred for 12 h and filtered through a pad of diatomaceous earth (Celite®). The filtrate was concentrated and the residue was subjected to flash chromatography to give 1.35 g of the title compound of Step C as brown solid melting at 154°-157° C. ¹ H NMR (CDCl₃, 400 MHz): δ 7.33 (d,2H), 6.87 (d,2H), 6.82 (dd,1H, J=11.3 and 8.75 Hz), 5.91 (dd,1H, J=8.5 and 3.5 Hz), 4.65 (s,2H), 4.22 (s,2H), 3.79 (s,3H), 3.75 (br s,2H).

Step D

7-Chloro-5-fluoro-1,3-dihydro-1- (4-methoxphenyl)methyl!-2,1-benzisothiazol-4-amine 2,2-dioxide

A mixture of the title compound of Step C (0.387 g, 1.2 mmol) and N-chlorosuccinimide (0.168 g, 1.26 mmol) in dimethylformamide (6 mL) was heated at 80° C. for 4 h. After completion of the reaction, the mixture was poured into a mixture of ether (25 mL) and water (10 mL). The organic phase was separated, dried (MgSO₄) and the solvent was removed on a rotary evaporator. Flash chromatography of the resulting residue afforded 0.4 g of the title compound of Step D. ¹ H NMR (CDCl₃, 400 MHz): δ 7.23 (d,2H), 7.03 (d,1H), 6.74 (d,2H), 4.93 (s,2H), 3.84 (s,2H), 3.75 (s,3H).

Step E

2- 7-Chloro-5-fluoro-1,3-dihydro-1- (4-methoxyphenyl)methyl!-2,1-benzisothiazol-4-yl!4,5,6,7-tetrahydro-1 H-isoindole-1,3(2H)-dione S,S-dioxide and 2-(7-chloro-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione S,S-dioxide

A mixture of the title compound of Step D (0.43 g, 1.2 mmol) and 3,4,5,6-tetrahydrophthalic anhydride (0.183 g, 1.2 mmol) in acetic acid (10 mL) was heated at reflux for 36 h. The solvent was then removed under reduced pressure and flash chromatography using 1-chlorobutane:ether (9:1) as eluent gave two compounds. 2- 7-Chloro-5-fluoro-1,3-dihydro-1- (4-methoxyphenyl)methyl!-2,1-benzisothiazol-4-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3 (2H)-dione S,S-dioxide, a compound of the invention, was eluted first as a solid melting at 171°-174° C. ¹ H NMR (CDCl₃, 300 MHz): δ 7.22-7.27 (m,3H), 6.80 (dd,2H, J=8.63 and 2.06 Hz), 4.98 (s,2H), 3.99 (s,2H), 3.77 (s,3H), 2.41 (m,4H), 1.81 (m,4H). 2-(7-Chloro-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione S,S-dioxide, a compound of the invention, was eluted second as a solid melting at 75°-79° C. ¹ H NMR (CDCl₃, 300 MHz): δ 7.21 (d,1H, 9.38 Hz), 7.13 (br s,1H), 4.38 (s,2H), 2.44 (m,4H), 1.84 (m,4H).

EXAMPLE 14 2-(1-Acetyl-7-chloro-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-yl)-4,5,6,7-tetrahydro- 1H-isoindole-1,3(2H)-dione S,S-dioxide

To a solution of 2-(7-chloro-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3-(2H)-dione S,S-dioxide (0.208 g, 0.56 mmol) and Et₃ N (0.5 mL) in anhydrous tetrahydrofuran (5 mL) was added acetyl chloride (50 mg, 0.044 mmol) dropwise at 0° C. The reaction mixture was then stirred at room temperature for 4 h. After the reaction was complete (TLC), the solvent was removed and the title compound of Example 14, a compound of the invention, was isolated by flash chromatography as a solid melting at 205°-208° C. ¹ H NMR (CDCl₃, 300 MHz): δ 7.37 (d,1H, J=9.57 Hz), 4.38 (s,2H), 2.59 (s,3H), 2.44 (m,4H) and 1.84 (m,4H).

EXAMPLE 15

Step A

7-Chloro-5-fluoro-1,3-dihydro-4-isocyanato-1- (4-methoxphenyl)methyl!-2,1-benzisothiazol 2,2-dioxide

Following the procedures described in Step A in Example 4 using the title compound of Step D in Example 13 (0.68 g, 2 mmol), diphosgene (2.2 mmol) and triethylamine (3 mmol) afforded the title compound of Step A.

Step B

3- 7-Chloro-5-fluoro-1,3-dihydro-1- (4-methoxyphenyl)methyl-!2,1 -benzisothiazol-4-yl!-6-(trifluoromethyl)-2,4(1H,3H)-i pyrimidinedione S,S-dioxide

A solution of ethyl 3-amino-4,4,4-trifluorocrotonate (0.627 g, 3.42 mmol) in DMF (5 mL) was added to sodium hydride (137 mg, 60% suspension in oil) at -10° to -5° C. The reaction mixture was stirred initially at -10° to -5° C. for 30 min, and then cooled to -78° C. The reaction mixture was stirred for 2 h and warmed to room temperature with continued stirring for 12 h. The reaction mixture was then poured into ice cold aqueous HCl (10 mL of conc. HCl and 18 g of ice) and extracted with ethyl acetate (25 mL). The organic extract was dried (MgSO₄) and concentrated. The title compound of Step B, a compound of the invention, was isolated by flash chromatography as a solid melting at >230° C. ¹ H NMR (Me₂ SO-d₆, 400 MHz): δ 12.75 (br s,1H), 7.80 (d,1H), 7.27 (d,2H), 6.88 (d,2H), 6.45 (s,1H), 4.89 (s,2H), 486 (d,1H), 4.54 (d,1H), 3.72 (s,3H).

EXAMPLE 16 3- 7-Chloro-5-fluoro-1,3-dihydro-1- (4-methoxphenyl)methyl!-2,1-benzisothiazol-4-yl!-1-methyl-6-(trifluoromethyl)-2,4(1H3H)-pyrimidinedione S,S-dioxide

A mixture of the title compound of Step B in Example 15 (0.948 g, 1.82 mmol), dimethyl sulfate (0.24 g, 1.91 mmol) and K₂ CO₃ (0.504 g, 3.65 mmol) in acetone (10 mL) was heated at reflux for 3 h. After the reaction was complete (TLC), the reaction mixture was cooled, insolubles were filtered off and the filtrate was concentrated on a rotary evaporator to give a solid. The title compound of Example 16, a compound of the invention, was isolated by flash chromatography as a solid melting at 180°-182° C. ¹ H NMR (CDCl₃, 300 MHz): δ 7.27 (m,3H), 6.81 (m,2H), 6.31 (s,1H), 4.98 (s,2H), 3.94 (d,2H), 3.77 (s,3H), 3.54 (s,3H).

EXAMPLE 17 3-(7-Chloro-5-fluoro-1,3-dihydro-2,1 -benzisothiazol-4-yl)-1-methyl-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedione S,S-dioxide

To a solution of the title compound of Example 16 (0.12 g, 0.225 mmol) in ethyl acetate (3 mL) was added conc. H₂ SO₄ (3 mL) at -10° C. The reaction mixture was stirred at 0° C. for 1 h. After the reaction was complete (TLC), the reaction mixture was poured into a mixture of ice (60 g) and ethyl acetate (400 mL). The organic phase was separated, washed with water (2×50 mL), dried (MgSO₄) and concentrated. The title compound of Example 17, a compound of the invention, was isolated by flash chromatography as a solid melting at >230° C. ¹ H NMR (Me₂ SO-d₆, 400 MHz): δ 11.18 (bs,1H), 7.68 (d,1H), 6.62 (s,1H), 4.58 (q,2H), 3.42 (s,3H).

EXAMPLE 18 1-Acetyl-7-chloro-4- 3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1(2H)-pyrimidinyl!-5-fluoro-1,3-dihydro-2,1-benzisothiazole 2,2-dioxide

To a solution of the title compound of Example 17 (0.1 g, 0.253 mmol), triethylamine (38.5 mg, 0.38 mmol) and pyridine (0.1 g) in tetrahydrofuran (4 mL) was added acetyl chloride (0.022 mL, 0.304 mmol) and the reaction mixture was stirred initially at 0° C. and then at room temperature for 1 h. After the reaction was complete, the solvents were removed and the title compound of Example 18, a compound of the invention, was isolated by flash chromatography as a colorless solid melting at 213°-215° C. ¹ H NMR (CDCl₃, 300 MHz): δ 7.40 (d,1H), 6.37 (s,1H), 4.33 (s,2H), 3.57 (s,3H), 2.59 (s,3H).

EXAMPLE 19

Step A

4-Fluoro-1-nitro-2-(phenylmethoxy) benzene

A mixture of 5-fluoro-2-nitrophenol (28 g, 0.178 mol), benzyl bromide (33.53 g, 0.195 mol) and K₂ CO₃ (30.8 g, 0.223 mol) in anhydrous DMF (150 mL) was stirred at room temperature for 12 h. After the reaction was complete, the reaction mixture was poured into a mixture of ether (1000 mL) and water (200 mL). The organic phase was separated, washed with water (3×100 mL), dried (MgSO₄) and concentrated to give the title compound of Step A (40.5 g).

Step B

4-Fluoro-2-(phenylmethoxy)benzenamine

To a mixture of iron powder (90.36 g, 1.62 mol) and acetic acid (10%, 400 mL) at 80° C. was added a solution of the title compound of Step A (40 g, 0.162 mol) in ethyl acetate (200 mL) dropwise with vigorous stirring. The reaction mixture was stirred further at 76° C. for 1 h. After the reaction was complete, the hot reaction mixture was filtered through Celite® (200 g) and the filter cake was washed with ethyl acetate (1000 mL). The filtrate was washed with water (3×200 mL), sodium bicarbonate solution (5%, 3×200 mL), dried (MgSO₄) and concentrated to give the crude product. The product was purified by flash chromatography to give 24.76 g of the title compound of Step B. ¹ H NMR (CDCl₃, 400 MHz): δ 7.41 (m,5H), 6.60 (m,3H), 5.04 (s,2H).

Step C

1 -Chloro-N-(4-fluoro-2-hydroxphenyl)methanesulfonamide

To a mixture of the title compound of Step B (13 g, 59.8 mmol) in pyridine (60 mL) at 0° C. was added chloromethylsulfonyl chloride (8.92 g, 59.8 mmol) dropwise at 0° C. under a nitrogen atmosphere. The reaction mixture was then stirred at 0° C. for 1.5 h and at room temperature for 6 h. After the reaction was complete (TLC), the reaction mixture was poured into ethyl acetate (750 mL) containing dilute HCl (10%, 150 mL). The organic phase was separated, washed successively with water (2×100 mL), dilute HCl (2×100 mL) and water (2×100 mL). After drying (MgSO₄), the organic layer was concentrated under reduced pressure to give 10.8 g of a solid melting at 87°-90° C. A suspension of this solid (10.5 g, 31.8 mmol) and Pd-C (10%, 1.0 g) in THF (60 mL) was hydrogenated using a Parr-shaker at 40 psi for 6 h. After the reaction was complete, the catalyst was filtered and the filtrate was concentrated to give 7.6 g of the title compound of Step C as a solid melting at 141°-143° C. ¹ H NMR (CDCl₃, 300 MHz): δ 7.28 (dd,1H), 6.6 (dd,1H), 6.64 (m,1H), 4.52 (s,2H).

Step D

6-Fluoro-1H-4,2,1-benzoxathiazine 2,2-dioxide

A mixture of the title compound of Step C (0.985 g, 4.11 mmol) and K₂ CO₃ (0.625 g, 4.52 mmol) in DMF (5 mL) was heated at 100° C. for 4 h. After the starting material had been consumed (TLC), the reaction mixture was poured into an ethyl acetate (50 mL) and water (10 mL) mixture. The organic phase was washed with water (2×10 mL), dried (MgSO₄), and concentrated. The product was purified by flash chromatography to give 0.42 g of the title compound of Step D as yellow solid. ¹ H NMR (CDCl₃, 300 MHz): δ 6.8 (m,3H), 6.2 (s,1H, NH), 4.95 (s,2H). IR (CDCl₃) 3347, 1506, 1148 cm-⁻¹.

Step E

6-Fluoro-1-(phenylmethyl)-1H-4,2,1-benzoxathiazine 2,2-dioxide

A mixture of the title compound of Step D (0.5 g, 2.46 mmol), K₂ CO₃ (1.02 g, 7.38 mmol), benzyl bromide (0.463 g, 2.71 mmol) and TBAB (79 mg) in DMF (5 mL) was stirred at room temperature for 48 h. After the reaction was complete, the reaction mixture was poured into an H₂ O/ethyl acetate mixture (10/100 mL). The organic phase was separated, dried and concentrated to give the title compound of Step E as a brown solid (0.76 g). ¹ H NMR (CDCl₃, 300 MHz): δ 7.32 (m,6H, aromatic) 6.72 (d,1H, 11 Hz), 6.34 (d,1H, 8 Hz), 4.82 (s,2H), 4.69 (s,2H).

Step F

6-Fluoro-7-nitro-1-(phenylmethyl)-1H-4,2,1-benzoxathiazine 2,2-dioxide and 6-Fluoro-7-nitro-1- (4-nitrophenyl)methyl!-1H-4,2,1-benzoxathiazine 2,2-dioxide

To a solution of the title compound of Step E (0.76 g, 2.46 mmol) in acetic acid (20 mL) and H₂ SO₄ (80%, 11.4 mL) was added nitric acid (2.9 mL, 70% HNO₃ +0.3 mL H₂ O) at 0° C. and resulting reaction mixture was stirred initially at 0° C. for 1 h and then at room temperature for 1.5 h. After the reaction was complete, the mixture was poured into ice water (50 mL) and extracted with ethyl acetate (100 mL). The organic extract was washed with water (2×10 mL), dried and concentrated. The two resulting products were separated by flash chromatography. The first compound eluted was 6-fluoro-7-nitro-1-(phenylmethyl)-1H-4,2,1-benzoxathiazine 2,2-dioxide (0.29 g) as a solid melting at 128°-130° C. ¹ H NMR (CDCl₃, 400 MHz): δ 7.80 (d,1H, J=7 Hz), 7.30-7.39 (m,5H), 6.93 (d,1H, J=10.5 Hz), 4.99 (s,2H), 4.88 (s,2H). The second compound eluted was 6-fluoro-7-nitro-1- (4-nitrophenyl)methyl!-1H-4,2,1 -benzoxathiazine 2,2-dioxide (0.296 gm) as a solid melting at 119°-122° C.

Step G

6-Fluoro-1-(phenylmethyl)-1H-4,2,1-benzoxathiazine-7-amine 2,2-dioxide

A mixture of 6-fluoro-7-nitro-1-(phenylmethyl)-1H-4,2,1-benzoxathiazine 2,2-dioxide (1.96 g, 5.79 mmol) and SnCl₂.2H₂ O (6.55 g, 29 mmol) in ethyl acetate (40 mL) was heated at reflux for 3 h. After the reaction was complete, ethyl acetate (400 mL) and then Na₂ CO₃ (18.5 g) were added, and the mixture was stirred for 12 h. The resulting mixture was filtered and the filtrate was concentrated under reduced pressure to give 1.20 g of the title compound of Step G.

Step H

2- 6-Fluoro-1-(phenylmethyl)-1H-4,2,1-benzoxathiazin-7-yl!-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H )-dione S,S-dioxide

A mixture of the title compound of Step G (1.2 g, 3.89 mmol), 3,4,5,6-tetrahydrophthalic anhydride (0.59 g) and acetic acid (6 mL) was heated at reflux for 48 h. After the reaction was complete, the reaction mixture was poured into an ethyl acetate (100 mL) and water (20 mL) mixture. The organic layer was separated, dried, and concentrated. Flash chromatography of the residue afforded 1.17 g of the title compound of Step H, a compound of the invention, as a colorless solid melting at 150°-152° C. ¹ H NMR (CDCl₃, 300 MHz): δ 7.33 (m,5H), 6.89 (m,2H), 4.92 (s,2H), 4.79 (s,2H), 2.41 (m,4H), 1.81 (m,4H).

By the procedures described herein, the following compounds of Tables 1-19 can be prepared. The following abbreviations are used: Ph=phenyl, c=cyclo, t=tertiary, Me=methyl. All allyl groups are the normal isomers unless indicated otherwise.

                                      TABLE 1     __________________________________________________________________________     Compounds of Formula I wherein R.sup.1 = F, R.sup.2 = Cl, R.sup.4 =     R.sup.5 = H, J = J - 1,     Z = CH.sub.2, R.sup.9 = R.sup.10 = H, n = 1, m = 2,     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-propyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 OCH.sub.2 CH.sub.2 OCH.sub.2     CH.sub.3            c-hexyl                   CH.sub.3 OCH.sub.2 CH.sub.2                          (4-MeO-Ph)CH.sub.2                                  Cl.sub.3 CCH.sub.2 OC(=O)     ethyl  FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 S(O).sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     propyl CHF.sub.2                   CH.sub.3 C(=O)                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 NHC(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     Compounds of Formula II wherein R.sup.1 = F, R.sup.4 = R.sup.5 = H, J = J     - 1, Z = CH.sub.2,     R.sup.9 = R.sup.10 = H, n = 1, m = 2, X = direct bond,     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-propyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 OCH.sub.2 CH.sub.2 OCH.sub.2     CH.sub.3            c-hexyl                   CH.sub.3 OCH.sub.2 CH.sub.2                          (4-MeO-Ph)CH.sub.2                                  Cl.sub.3 CCH.sub.2 OC(=O)     ethyl  FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 S(O).sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     propyl CHF.sub.2                   CH.sub.3 C(=O)                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 NHC(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     X = O,     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-propyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 OCH.sub.2 CH.sub.2 OCH.sub.2     CH.sub.3            c-hexyl                   CH.sub.3 OCH.sub.2 CH.sub.2                          (4-MeO-Ph)CH.sub.2                                  Cl.sub.3 CCH.sub.2 OC(=O)     ethyl  FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 S(O).sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     propyl CHF.sub.2                   CH.sub.3 C(=O)                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 NHC(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     X = S,     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-propyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 OCH.sub.2 CH.sub.2 OCH.sub.2     CH.sub.3            c-hexyl                   CH.sub.3 OCH.sub.2 CH.sub.2                          (4-MeO-Ph)CH.sub.2                                  Cl.sub.3 CCH.sub.2 OC(=O)     ethyl  FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 S(O).sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     propyl CHF.sub.2                   CH.sub.3 C(=O)                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 NHC(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     X = NH,     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-propyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 OCH.sub.2 CH.sub.2 OCH.sub.2     CH.sub.3            c-hexyl                   CH.sub.3 OCH.sub.2 CH.sub.2                          (4-MeO-Ph)CH.sub.2                                  Cl.sub.3 CCH.sub.2 OC(=O)     ethyl  FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 S(O).sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     propyl CHF.sub.2                   CH.sub.3 C(=O)                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 NHC(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     X = NCH.sub.3,     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-propyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 OCH.sub.2 CH.sub.2 OCH.sub.2     CH.sub.3            c-hexyl                   CH.sub.3 OCH.sub.2 CH.sub.2                          (4-MeO-Ph)CH.sub.2                                  Cl.sub.3 CCH.sub.2 OC(=O)     ethyl  FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 S(O).sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     propyl CHF.sub.2                   CH.sub.3 C(=O)                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 NHC(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________

                                      TABLE 2     __________________________________________________________________________     Compounds of Formula I wherein R.sup.1 = F, R.sup.2 = Cl, R.sup.4 =     R.sup.5 = H, J = J - 2,     R.sup.9 = R.sup.10 = H, Z = CH.sub.2, m = 1, n = 2,     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-propyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 OCH.sub.2 CH.sub.2 OCH.sub.2     CH.sub.3            c-hexyl                   CH.sub.3 OCH.sub.2 CH.sub.2                          (4-MeO-Ph)CH.sub.2                                  Cl.sub.3 CCH.sub.2 OC(=O)     ethyl  FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 S(O).sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     propyl CHF.sub.2                   CH.sub.3 C(=O)                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 NHC(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     Z = CHF, n = 1, m = 1,     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-propyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 OCH.sub.2 CH.sub.2 OCH.sub.2     CH.sub.3            c-hexyl                   CH.sub.3 OCH.sub.2 CH.sub.2                          (4-MeO-Ph)CH.sub.2                                  Cl.sub.3 CCH.sub.2 OC(=O)     ethyl  FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 S(O).sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     propyl CHF.sub.2                   CH.sub.3 C(=O)                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 NHC(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     Z = O, n = 2, m = 1,     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-propyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 OCH.sub.2 CH.sub.2 OCH.sub.2     CH.sub.3            c-hexyl                   CH.sub.3 OCH.sub.2 CH.sub.2                          (4-MeO-Ph)CH.sub.2                                  Cl.sub.3 CCH.sub.2 OC(=O)     ethyl  FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 S(O).sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     propyl CHF.sub.2                   CH.sub.3 C(=O)                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 NHC(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     Compounds of Formula II wherein R.sup.1 = F, R.sup.4 = R.sup.5 = H, J = J     - 2,     Z = CH.sub.2, R.sup.9 = R.sup.10 = H, n = 1, m = 2, Z = CH.sub.2,     X = direct bond.     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-propyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 OCH.sub.2 CH.sub.2 OCH.sub.2     CH.sub.3            c-hexyl                   CH.sub.3 OCH.sub.2 CH.sub.2                          (4-MeO-Ph)CH.sub.2                                  Cl.sub.3 CCH.sub.2 OC(=O)     ethyl  FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 S(O).sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     propyl CHF.sub.2                   CH.sub.3 C(=O)                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 NHC(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     X = O,     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-propyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 OCH.sub.2 CH.sub.2 OCH.sub.2     CH.sub.3            c-hexyl                   CH.sub.3 OCH.sub.2 CH.sub.2                          (4-MeO-Ph)CH.sub.2                                  Cl.sub.3 CCH.sub.2 OC(=O)     ethyl  FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 S(O).sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     propyl CHF.sub.2                   CH.sub.3 C(=O)                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 NHC(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     X = S,     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-propyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 OCH.sub.2 CH.sub.2 OCH.sub.2     CH.sub.3            c-hexyl                   CH.sub.3 OCH.sub.2 CH.sub.2                          (4-MeO-Ph)CH.sub.2                                  Cl.sub.3 CCH.sub.2 OC(=O)     ethyl  FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 S(O).sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     propyl CHF.sub.2                   CH.sub.3 C(=O)                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 NHC(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     X = NH,     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-propyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 OCH.sub.2 CH.sub.2 OCH.sub.2     CH.sub.3            c-hexyl                   CH.sub.3 OCH.sub.2 CH.sub.2                          (4-MeO-Ph)CH.sub.2                                  Cl.sub.3 CCH.sub.2 OC(=O)     ethyl  FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 S(O).sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     propyl CHF.sub.2                   CH.sub.3 C(=O)                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 NHC(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     X = NCH.sub.3,     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-propyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 OCH.sub.2 CH.sub.2 OCH.sub.2     CH.sub.3            c-hexyl                   CH.sub.3 OCH.sub.2 CH.sub.2                          (4-MeO-Ph)CH.sub.2                                  Cl.sub.3 CCH.sub.2 OC(=O)     ethyl  FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 S(O).sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     propyl CHF.sub.2                   CH.sub.3 C(=O)                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 NHC(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________

                                      TABLE 3     __________________________________________________________________________     Compounds of Formula I wherein J = J - 3, R.sup.1 = F, R.sup.2 = Cl,     R.sup.4 = R.sup.5 = H,     R.sup.11 = CF.sub.2 H, R.sup.12 = CH.sub.3.     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-propyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 OCH.sub.2 CH.sub.2 OCH.sub.2     CH.sub.3            c-hexyl                   CH.sub.3 OCH.sub.2 CH.sub.2                          (4-MeO-Ph)CH.sub.2                                  Cl.sub.3 CCH.sub.2 OC(=O)     ethyl  FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 S(O).sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     propyl CHF.sub.2                   CH.sub.3 C(=O)                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 NHC(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     Compounds of Formula II wherein J = J - 3, R.sup.1 = F, R.sup.4 = R.sup.5     = H,     R.sup.11 = CF.sub.2 H, R.sup.12 = CH.sub.3, X = Direct Bond.     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-hexyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 NHC(=O)     CH.sub.3            FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 OCH.sub.2 CH.sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     ethyl  CHF.sub.2                   CH.sub.3 S(O).sub.2                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 C(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     X=O,     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-hexyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 NHC(=O)     CH.sub.3            FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 OCH.sub.2 CH.sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     ethyl  CHF.sub.2                   CH.sub.3 S(O).sub.2                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 C(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________

                                      TABLE 4     __________________________________________________________________________     Compounds of Formula I wherein J = J - 4, R.sup.1 = F, R.sup.2 = Cl,     R.sup.4 = R.sup.5 = H,     Q = O, R.sup.13 =  CH.sub.3, W = CH, R.sup.14 =  CF.sub.3,     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-hexyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 NHC(=O)     CH.sub.3            FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 OCH.sub.2 CH.sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     ethyl  CHF.sub.2                   CH.sub.3 S(O).sub.2                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 C(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     W = N, R.sup.14 = N(CH.sub.3).sub.2,     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-hexyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 NHC(=O)     CH.sub.3            FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 OCH.sub.2 CH.sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     ethyl  CHF.sub.2                   CH.sub.3 S(O).sub.2                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 C(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     Compounds of Formula II wherein J = J - 4, R.sup.1 = F, R.sup.4 = R.sup.5     = H,     Q = O, R.sup.13 = CH.sub.3, X = Direct Bond, W = CH, R.sup.14     = CF.sub.3,     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-hexyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 NHC(=O)     CH.sub.3            FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 OCH.sub.2 CH.sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     ethyl  CHF.sub.2                   CH.sub.3 S(O).sub.2                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 C(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     X = O, W = N, R.sup.14 = (CH.sub.3).sub.2,     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-hexyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 NHC(=O)     CH.sub.3            FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 OCH.sub.2 CH.sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     ethyl  CHF.sub.2                   CH.sub.3 S(O).sub.2                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 C(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________

                                      TABLE 5     __________________________________________________________________________     Compounds of Formula I wherein J = J - 5, R.sup.1 = F, R.sup.2 = Cl,     R.sup.4 = R.sup.5 = H,     Q = O, R.sup.9 = R.sup.10 = H, Z = CH.sub.2, only single bonds in     left-hand ring,     n = m = 1,     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-hexyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 NHC(=O)     CH.sub.3            FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 OCH.sub.2 CH.sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     ethyl  CHF.sub.2                   CH.sub.3 S(O).sub.2                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 C(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     m = 2, n = 1,     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-hexyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 NHC(=O)     CH.sub.3            FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 OCH.sub.2 CH.sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     ethyl  CHF.sub.2                   CH.sub.3 S(O).sub.2                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 C(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     Compounds of Formula II wherein J = J - 5, R.sup.1 = F, R.sup.4 = R.sup.5     = H,     Q = O, R.sup.9 = R.sup.10 = H, Z = CH.sub.2, only     single bonds in left-hand ring.     X = Direct Bond, n = m = 1,     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-hexyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 NHC(=O)     CH.sub.3            FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 OCH.sub.2 CH.sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     ethyl  CHF.sub.2                   CH.sub.3 S(O).sub.2                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 C(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     X = O, m = 2, n = 1,     R.sup.3            R.sup.3                   R.sup.3                          R.sup.3 R.sup.3     __________________________________________________________________________     H      c-hexyl                   CH.sub.3 OCH.sub.2                          PhCH.sub.2 OC(=O)                                  CH.sub.3 NHC(=O)     CH.sub.3            FCH.sub.2 CH.sub.2 CH.sub.2                   CH.sub.3 OCH.sub.2 CH.sub.2                          PhCH.sub.2                                  ClCH.sub.2 CH.sub.2 CH.sub.2     ethyl  CHF.sub.2                   CH.sub.3 S(O).sub.2                          propargyl                                  (CH.sub.3).sub.3 COC(=O)     octyl  allyl  CH.sub.3 C(=O)                          CH.sub.3 NHS(O).sub.2                                  CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________

                                      TABLE 6     __________________________________________________________________________     Compounds of Formula I wherein J = J-6, R.sup.1 = F, R.sup.2 = Cl,     R.sup.4 =     R.sup.5 = H, Q = O, R.sup.16 = R.sup.17 = H, only single bonds in     left-hand ring,     R.sup.3         R.sup.3 R.sup.3 R.sup.3 R.sup.3     __________________________________________________________________________     Z.sup.1 = CH.sub.2, n = m = 1,     H   c-hexyl CH.sub.3 OCH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2                                 ClCH.sub.2 CH.sub.2 CH.sub.2     ethyl         CHF.sub.2                 CH.sub.3 S(O).sub.2                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     octyl         allyl   CH.sub.3 C(═O)                         CH.sub.3 NHS(O).sub.2                                 CH.sub.2 = CHCH.sub.2 CH.sub.2 CH.sub.2     Z.sup.1 = CHF, n = m = 1,     H   c-hexyl CH.sub.3 OCH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2                                 ClCH.sub.2 CH.sub.2 CH.sub.2     ethyl         CHF.sub.2                 CH.sub.3 S(O).sub.2                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     octyl         allyl   CH.sub.3 C(═O)                         CH.sub.3 NHS(O).sub.2                                 CH.sub.2 = CHCH.sub.2 CH.sub.2 CH.sub.2     Z.sup.1 = CF.sub.2, Z.sup.1 = CF.sub.2, n = m = 1,     H   c-hexyl CH.sub.3 OCH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2                                 ClCH.sub.2 CH.sub.2 CH.sub.2     ethyl         CHF.sub.2                 CH.sub.3 S(O).sub.2                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     octyl         allyl   CH.sub.3 C(═O)                         CH.sub.3 NHS(O).sub.2                                 CH.sub.2 = CHCH.sub.2 CH.sub.2 CH.sub.2     Z.sup.1 = O, n = 2, m = 1     H   c-hexyl CH.sub.3 OCH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2                                 ClCH.sub.2 CH.sub.2 CH.sub.2     ethyl         CHF.sub.2                 CH.sub.3 S(O).sub.2                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     octyl         allyl   CH.sub.3 C(═O)                         CH.sub.3 NHS(O).sub.2                                 CH.sub.2 = CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     Compounds of Formula II wherein J = J - 6, R.sup.1 = F, R.sup.4 = R.sup.5     = H,     Q = O, R.sup.16 = R.sup.17 = H, n = m = 1, only single bonds in left-hand     ring,     R.sup.3         R.sup.3 R.sup.3 R.sup.3 R.sup.3     __________________________________________________________________________     X = Direct Bond, Z.sup.1 = CH.sub.2,     H   c-hexyl CH.sub.3 OCH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2                                 ClCH.sub.2 CH.sub.2 CH.sub.2     ethyl         CHF.sub.2                 CH.sub.3 S(O).sub.2                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     octyl         allyl   CH.sub.3 C(═O)                         CH.sub.3 NHS(O).sub.2                                 CH.sub.2 = CHCH.sub.2 CH.sub.2 CH.sub.2     X = NCH.sub.3, Z.sup.1 = CH.sub.2,     H   c-hexyl CH.sub.3 OCH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2                                 ClCH.sub.2 CH.sub.2 CH.sub.2     ethyl         CHF.sub.2                 CH.sub.3 S(O).sub.2                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     octyl         allyl   CH.sub.3 C(═O)                         CH.sub.3 NHS(O).sub.2                                 CH.sub.2 = CHCH.sub.2 CH.sub.2 CH.sub.2     X = Direct Bond, Z.sup.1 = CHF,     H   c-hexyl CH.sub.3 OCH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2                                 ClCH.sub.2 CH.sub.2 CH.sub.2     ethyl         CHF.sub.2                 CH.sub.3 S(O).sub.2                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     octyl         allyl   CH.sub.3 C(═O)                         CH.sub.3 NHS(O).sub.2                                 CH.sub.2 =CHCH.sub.2 CH.sub.2 CH.sub.2     X = NCH.sub.3, Z.sup.1 = CHF,     H   c-hexyl CH.sub.3 OCH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2                                 ClCH.sub.2 CH.sub.2 CH.sub.2     ethyl         CHF.sub.2                 CH.sub.3 S(O).sub.2                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     octyl         allyl   CH.sub.3 C(═O)                         CH.sub.3 NHS(O).sub.2                                 CH.sub.2 = CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________

                                      TABLE 7     __________________________________________________________________________     Compounds of Formula I wherein J = J - 7, R.sup.1 = F, R.sup.2 = Cl,     R.sup.4 =     R.sup.5 = H, Q = O, R.sup.12 = H,     R.sup.3         R.sup.11                 R.sup.3 R.sup.11                                 R.sup.3                                       R.sup.11     __________________________________________________________________________     H   H       FCH.sub.2 CH.sub.2 CH.sub.2                         CH.sub.3                                 CHF.sub.2                                       CH.sub.3     CH.sub.3         H       CH.sub.3 OCH.sub.2 CH.sub.2                         CH.sub.3                                 allyl H     ethyl         CH.sub.3                 CH.sub.3 S(O).sub.2                         FCH.sub.2 CH.sub.2 CH.sub.2                                 propargyl                                       FCH.sub.2 CH.sub.2 CH.sub.2     ethyl         FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 C(═O)                         FCH.sub.2 CH.sub.2 CH.sub.2                                 PhCH.sub.2                                       CH.sub.3     __________________________________________________________________________     Compounds of Formula II wherein J = J - 7, R.sup.1 = F, R.sup.4 = R.sup.5     = H,     Q = O, R.sup.12 = H,     R.sup.3         R.sup.11                 R.sup.3 R.sup.11                                 R.sup.3                                       R.sup.11     __________________________________________________________________________     X = Direct Bond,     H   H       FCH.sub.2 CH.sub.2 CH.sub.2                         CH.sub.3                                 CHF.sub.2                                       CH.sub.3     CH.sub.3         H       CH.sub.3 OCH.sub.2 CH.sub.2                         CH.sub.3                                 allyl H     ethyl         CH.sub.3                 CH.sub.3 S(O).sub.2                         FCH.sub.2 CH.sub.2 CH.sub.2                                 propargyl                                       FCH.sub.2 CH.sub.2 CH.sub.2     ethyl         FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 C(═O)                         FCH.sub.2 CH.sub.2 CH.sub.2                                 PhCH.sub.2                                       CH.sub.3     X = NCH.sub.3,     H   H       FCH.sub.2 CH.sub.2 CH.sub.2                         CH.sub.3                                 CHF.sub.2                                       CH.sub.3     CH.sub.3         H       CH.sub.3 OCH.sub.2 CH.sub.2                         CH.sub.3                                 allyl H     ethyl         CH.sub.3                 CH.sub.3 S(O).sub.2                         FCH.sub.2 CH.sub.2 CH.sup.2                                 propargyl                                       FCH.sub.2 CH.sub.2 CH.sub.2     ethyl         FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 C(═O)                         FCH.sub.2 CH.sub.2 CH.sub.2                                 PhCH.sub.2                                       CH.sub.3     __________________________________________________________________________

                                      TABLE 8     __________________________________________________________________________     Compounds of Formula I wherein J = J - 8, R.sup.1 = F, R.sup.2 = Cl,     R.sup.4 =     R.sup.5 = H, R.sup.18 = t-butyl,     R.sup.3         R.sup.3 R.sup.3 R.sup.3 R.sup.3     __________________________________________________________________________     H   c-hexyl CH.sub.3 OCH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2                                 C1CH.sub.2 CH.sub.2 CH.sub.2     ethyl         CHF.sub.2                 CH.sub.3 S(O).sub.2                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     octyl         allyl   CH.sub.3 C(═O)                         CH.sub.3 NHS(O).sub.2                                 CH.sub.2 ═CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     Compounds of Formula II wherein J = J - 8, R.sup.1 = F, R.sup.4 = R.sup.5     = H,     R.sup.18 = t-butyl, X = O,     R.sup.3         R.sup.3 R.sup.3 R.sup.3 R.sup.3     __________________________________________________________________________     H   c-hexyl CH.sub.3 OCH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2                                 ClCH.sub.2 CH.sub.2 CH.sub.2     ethyl         CHF.sub.2                 CH.sub.3 S(O).sub.2                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     octyl         allyl   CH.sub.3 C(═O)                         CH.sub.3 NHS(O).sub.2                                 CH.sub.2 ═CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________

                                      TABLE 9     __________________________________________________________________________     Compounds of Formula I wherein J = J - 9, R.sup.1 = F, R.sup.2 = Cl,     R.sup.4 =      R.sup.5 = H, Q = O, R.sup.18 = CH.sub.2 CH.sub.2 CH.sub.2 F,     R.sup.3         R.sup.3 R.sup.3 R.sup.3 R.sup.3     __________________________________________________________________________     H   c-hexyl CH.sub.3 OCH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2                                 ClCH.sub.2 CH.sub.2 CH.sub.2     ethyl         CHF.sub.2                 CH.sub.3 S(O).sub.2                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     octyl         allyl   CH.sub.3 C(═O)                         CH.sub.3 NHS(O).sub.2                                 CH.sub.2 ═CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________     Compounds of Formula II wherein J = J - 9, R.sup.1 = F, R.sup.4 = R.sup.5     = H,     Q = O, R.sup.18 = CH.sub.2 CH.sub.2 CH.sub.2 F, X = O,     R.sup.3         R.sup.3 R.sup.3 R.sup.3 R.sup.3     __________________________________________________________________________     H   c-hexyl CH.sub.3 OCH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2                                 ClCH.sub.2 CH.sub.2 CH.sub.2     ethyl         CHF.sub.2                 CH.sub.3 S(O).sub.2                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     octyl         allyl   CH.sub.3 C(═O)                         CH.sub.3 NHS(O).sub.2                                 CH.sub.2 ═CHCH.sub.2 CH.sub.2 CH.sub.2     __________________________________________________________________________

                                      TABLE 10     __________________________________________________________________________     Compounds of Formula I wherein J = J - 10, R.sup.1 = F, R.sup.2 = Cl,     R.sup.4 =     R.sup.5 = H, Q = O, R.sup.9 = R.sup.10 = H, Z = CH.sub.2,     m = n = 1, R.sup.19 = R.sup.20 = H,     R.sup.3         R.sup.3  R.sup.3 R.sup.3  R.sup.3     __________________________________________________________________________     H   FCH.sub.2 CH.sub.2 CH.sub.2                  CH.sub.3 OCH.sub.2 CH.sub.2                          PhCH.sub.2 OC(═O)                                   CH.sub.3 NHC(═O)     CH.sub.3         CHF.sub.2                  CH.sub.3 S(O).sub.2                          PhCH.sub.2                                   octyl     ethyl         allyl    CH.sub.3 C(═O)                          propargyl                                   (CH.sub.3).sub.3 COC(═O)     __________________________________________________________________________     Compounds of Formula II wherein J = J - 10, R.sup.1 = F, R.sup.4 =     R.sup.5 = H,     Q = O, R.sup.9 = R.sup.10 = H, Z = CH.sub.2, m = n = 1, R.sup.19 =     R.sup.20 = H, X = O,     R.sup.3         R.sup.3  R.sup.3 R.sup.3  R.sup.3     __________________________________________________________________________     H   FCH.sub.2 CH.sub.2 CH.sub.2                  CH.sub.3 OCH.sub.2 CH.sub.2                          PhCH.sub.2 OC(═O)                                   CH.sub.3 NHC(═O)     CH.sub.3         CHF.sub.2                  CH.sub.3 S(O).sub.2                          PhCH.sub.2                                   octyl     ethyl         allyl    CH.sub.3 C(═O)                          propargyl                                   (CH.sub.3).sub.3 COC(═O)     __________________________________________________________________________

                                      TABLE 11     __________________________________________________________________________     Compounds of Formula I wherein J = J - 12, R.sup.1 = F, R.sup.2 = Cl,     R.sup.4 =     R.sup.5 = H, Q = O, Q.sup.1 = S, R.sup.9 = R.sup.10 = H, Z =     CH.sub.2, m = n = 1, only single bonds in left-hand ring,     R.sup.3         R.sup.3  R.sup.3 R.sup.3  R.sup.3     __________________________________________________________________________     H   FCH.sub.2 CH.sub.2 CH.sub.2                  CH.sub.3 OCH.sub.2 CH.sub.2                          PhCH.sub.2 OC(═O)                                   CH.sub.3 NHC(═O)     CH.sub.3         CHF.sub.2                  CH.sub.3 S(O).sub.2                          PhCH.sub.2                                   octyl     ethyl         allyl    CH.sub.3 C(═O)                          propargyl                                   (CH.sub.3).sub.3 COC(═O)     __________________________________________________________________________     Compounds of Formula II wherein J = J - 12, R.sup.1 = F, R.sup.4 =     R.sup.5 = H,     Q = O, Q.sup.1 = S, R.sup.9 = R.sup.10 = H, X = O, m = n = 1,     only single bonds in left-hand ring,     R.sup.3         R.sup.3 R.sup.3 R.sup.3 R.sup.3     __________________________________________________________________________     Z = CH.sub.2,     H   FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         CHF.sub.2                 CH.sub.3 S(O).sub.2                         PhCH.sub.2                                 octyl     ethyl         allyl   CH.sub.3 C(═O)                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     Z = CHF,     H   FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         CHF.sub.2                 CH.sub.3 S(O).sub.2                         PhCH.sub.2                                 octyl     ethyl         allyl   CH.sub.3 C(═O)                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     __________________________________________________________________________

                                      TABLE 12     __________________________________________________________________________     Compounds of Formula I wherein J = J - 14, R.sup.1 = F, R.sup.2 = Cl,     R.sup.4 =     R.sup.5 = H, Q.sup.1 = S, R.sup.9 = R.sup.10 = H, Z = CH.sub.2,     m = 2, n = 1,     R.sup.3         R.sup.3 R.sup.3 R.sup.3 R.sup.3     __________________________________________________________________________     H   FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         CHF.sub.2                 CH.sub.3 S(O).sub.2                         PhCH.sub.2                                 octyl     ethyl         allyl   CH.sub.3 C(═O)                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     __________________________________________________________________________     Compounds of Formula II wherein J = J - 14, R.sup.1 = F, R.sup.4 =     R.sup.5 = H,     Q.sup.1 = S, R.sup.9 = R.sup.10 = H, Z = CH.sub.2, m = 2, n = 1,     X = O,     R.sup.3         R.sup.3  R.sup.3 R.sup.3  R.sup.3     __________________________________________________________________________     H   FCH.sub.2 CH.sub.2 CH.sub.2                  CH.sub.3 OCH.sub.2 CH.sub.2                          PhCH.sub.2 OC(═O)                                   CH.sub.3 NHC(═O)     CH.sub.3         CHF.sub.2                  CH.sub.3 S(O).sub.2                          PhCH.sub.2                                   octyl     ethyl         allyl    CH.sub.3 C(═O)                          propargyl                                   (CH.sub.3).sub.3 COC(═O)     __________________________________________________________________________

                                      TABLE 13     __________________________________________________________________________     Compounds of Formula I wherein J = J - 15, R.sup.1 = F, R.sup.2 = Cl,     R.sup.4 =     R.sup.5 = H, R.sup.9 = R.sup.10 = H, Z = CH.sub.2,m = 2, n = 1,     R.sup.23 = Cl,     R.sup.3         R.sup.3 R.sup.3 R.sup.3 R.sup.3     __________________________________________________________________________     H   FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         CHF.sub.2                 CH.sub.3 S(O).sub.2                         PhCH.sub.2                                 octyl     ethyl         allyl   CH.sub.3 C(═O)                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     __________________________________________________________________________     Compounds of Formula II wherein J = J - 15, R.sup.1 = F, R.sup.4 =     R.sup.5 = H,     R.sup.9 = R.sup.10 = H, Z = CH.sub.2, m = 2, n = 1, R.sup.23 = Cl,     R.sup.3         R.sup.3  R.sup.3 R.sup.3  R.sup.3     __________________________________________________________________________     X = Direct Bond,     H   FCH.sub.2 CH.sub.2 CH.sub.2                  CH.sub.3 OCH.sub.2 CH.sub.2                          PhCH.sub.2 OC(═O)                                   CH.sub.3 NHC(═O)     CH.sub.3         CHF.sub.2                  CH.sub.3 S(O).sub.2                          PhCH.sub.2                                   octyl     ethyl         allyl    CH.sub.3 C(═O)                          propargyl                                   (CH.sub.3).sub.3 COC(═O)     X = O,     H   FCH.sub.2 CH.sub.2 CH.sub.2                  CH.sub.3 OCH.sub.2 CH.sub.2                          PhCH.sub.2 OC(═O)                                   CH.sub.3 NHC(═O)     CH.sub.3         CHF.sub.2                  CH.sub.3 S(O).sub.2                          PhCH.sub.2                                   octyl     ethyl         allyl    CH.sub.3 C(═O)                          propargyl                                   (CH.sub.3).sub.3 COC(═O)     __________________________________________________________________________

                                      TABLE 14     __________________________________________________________________________     Compounds of Formula I wherein J = J - 16, R.sup.1 = F, R.sup.2 = Cl,     R.sup.4 =     R.sup.5 = H, R.sup.23 = Cl, R.sup.24 = CF.sub.3, R.sup.25 = CH.sub.3,     R.sup.3         R.sup.3 R.sup.3 R.sup.3 R.sup.3     __________________________________________________________________________     H   FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         CHF.sub.2                 CH.sub.3 S(O).sub.2                         PhCH.sub.2                                 octyl     ethyl         allyl   CH.sub.3 C(═O)                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     __________________________________________________________________________     Compounds of Formula II wherein J = J - 16, R.sup.1  = F, R.sup.4  =     R.sup.5  =     H, R.sup.23  = Cl, R.sup.24  = CF.sub.3, R.sup.25  = CH.sub.3,     R.sup.3         R.sup.3 R.sup.3 R.sup.3 R.sup.3     __________________________________________________________________________     X = Direct Bond,     H   FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         CHF.sub.2                 CH.sub.3 S(O).sub.2                         PhCH.sub.2                                 octyl     ethyl         allyl   CH.sub.3 C(═O)                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     X = O,     H   FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         CHF.sub.2                 CH.sub.3 S(O).sub.2                         PhCH.sub.2                                 octyl     ethyl         allyl   CH.sub.3 C(═O)                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     __________________________________________________________________________

                                      TABLE 15     __________________________________________________________________________     Compounds of Formula I wherein J = J - 17, R.sup.1 = F, R.sup.2 = C1,     R.sup.4 =     R.sup.5 = H, R.sup.9 = R.sup.10 = H, m = n = 1, R.sup.26 = CH.sub.3,     R.sup.3         R.sup.3 R.sup.3 R.sup.3 R.sup.3     __________________________________________________________________________     Z = CH.sub.2,     H   FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         CHF.sub.2                 CH.sub.3 S(O).sub.2                         PhCH.sub.2                                 octyl     ethyl         allyl   CH.sub.3 C(═O)                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     Z = CHF,     H   FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         CHF.sub.2                 CH.sub.3 S(O).sub.2                         PhCH.sub.2                                 octyl     ethyl         allyl   CH.sub.3 C(═O)                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     __________________________________________________________________________     Compounds of Formula II wherein J = J - 17, R.sup.1 = F, R.sup.4 =     R.sup.5 =     H, R.sup.9 = R.sup.10 = H, m = n = 1, R.sup.26 = CH.sub.3,     R.sup.3         R.sup.3 R.sup.3 R.sup.3 R.sup.3     __________________________________________________________________________     X = Direct Bond, Z = CH.sub.2,     H   FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         CHF.sub.2                 CH.sub.3 S(O).sub.2                         PhCH.sub.2                                 octyl     ethyl         allyl   CH.sub.3 C(═O)                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     X = O, Z = CH.sub.2,     H   FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         CHF.sub.2                 CH.sub.3 S(O).sub.2                         PhCH.sub.2                                 octyl     ethyl         allyl   CH.sub.3 C(═O)                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     X = O, Z = CHF,     H   FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         CHF.sub.2                 CH.sub.3 S(O).sub.2                         PhCH.sub.2                                 octyl     ethyl         allyl   CH.sub.3 C(═O)                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     __________________________________________________________________________

                                      TABLE 16     __________________________________________________________________________     Compounds of Formula I wherein J = J - 18, R.sup.1 = F, R.sup.2 = Cl,     R.sup.4 =     R.sup.5 = H, R.sup.9 = R.sup.10 = H, m = 2, n = 1,     R.sup.26 = CH.sub.3,     R.sup.3         R.sup.3 R.sup.3 R.sup.3 R.sup.3     __________________________________________________________________________     Z = CH.sub.2,     H   FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         CHF.sub.2                 CH.sub.3 S(O).sub.2                         PhCH.sub.2                                 octyl     ethyl         allyl   CH.sub.3 C(═O)                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     Z = CHF,     H   FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         CHF.sub.2                 CH.sub.3 S(O).sub.2                         PhCH.sub.2                                 octyl     ethyl         allyl   CH.sub.3 C(═O)                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     __________________________________________________________________________     Compounds of Formula II wherein J = J - 18, R.sup.1 = F, R.sup.4 =     R.sup.5 = H, R.sup.9 = R.sup.10 = H, m = n = 1, R.sup.26 = CH.sub.3,     R.sup.3         R.sup.3 R.sup.3 R.sup.3 R.sup.3     __________________________________________________________________________     X = O, Z = CH.sub.2,     H   FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         CHF.sub.2                 CH.sub.3 S(O).sub.2                         PhCH.sub.2                                 octyl     ethyl         allyl   CH.sub.3 C(═O)                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     X = O, Z = CHF,     H   FCH.sub.2 CH.sub.2 CH.sub.2                 CH.sub.3 OCH.sub.2 CH.sub.2                         PhCH.sub.2 OC(═O)                                 CH.sub.3 NHC(═O)     CH.sub.3         CHF.sub.2                 CH.sub.3 S(O).sub.2                         PhCH.sub.2                                 octyl     ethyl         allyl   CH.sub.3 C(═O)                         propargyl                                 (CH.sub.3).sub.3 COC(═O)     __________________________________________________________________________

                  TABLE 17     ______________________________________     Compounds of Formula I where in J = J - 1, R.sup.3 = ethyl, R.sup.4 =     R.sup.5 =     H, R.sup.9 = R.sup.10 = H, m = 2, n = 1, Z = CH.sub.2,     R.sup.1           R.sup.2                  R.sup.1                        R.sup.2                             R.sup.1                                 R.sup.2                                      R.sup.1                                          R.sup.2                                               R.sup.1                                                   R.sup.2     ______________________________________     H     Cl     Cl    F    Cl  Cl   F   Br   F   NO.sub.2     H     F      Br    Cl   Br  F    F   CF.sub.3                                               F   CN     ______________________________________     Compounds of Formula II wherein J = J - 1, R.sup.3 = ethyl, R.sup.4 =     R.sup.5 = H, R.sup.9 = R.sup.10 = H, m = 2, n = 1, Z = CH.sub.2,     R.sup.1           X      R.sup.1                        X    R.sup.1                                 X    R.sup.1                                          X    R.sup.1                                                   X     ______________________________________     H     O      Cl    O    Cl  S    F   O    F   direct bond     H     S      Br    O    Br  S    F   S    F   NCH.sub.3     ______________________________________

                  TABLE 18     ______________________________________     Compounds of Formula I wherein J = J - l, R.sup.1 = F, R.sup.2 = Cl,     R.sup.3 = ethyl,     R.sup.9 = R.sup.10 = H, m= 2, n= 1, Z = CH.sub.2,     R.sup.4         R.sup.5               R.sup.4                      R.sup.5                          R.sup.4                               R.sup.5                                    R.sup.4                                         R.sup.5                                                R.sup.4                                                     R.sup.5     ______________________________________     Cl  H     Br     H   CH.sub.3                               CH.sub.3                                    ethyl                                         H      H    C(═O)CH                                                     3     F   H     CH.sub.3                      H   H    CF.sub.3                                    H    S(O).sub.2 CH.sub.3                                                spiro-cyclopropyl     ______________________________________     Compounds of Formula II wherein J = J - 1, R.sup.1 = F, R.sup.3 = ethyl,     R.sup.9 = R.sup.10 = H, m = 2, n = 1, Z = CH.sub.2, X = O,     R.sup.4         R.sup.5               R.sup.4                      R.sup.5                          R.sup.4                               R.sup.5                                    R.sup.4                                         R.sup.5                                                R.sup.4                                                     R.sup.5     ______________________________________     Cl  H     Br     H   CH.sub.3                               CH.sub.3                                    ethyl                                         H      H    C(═O)CH                                                     3     F   H     CH.sub.3                      H   H    CF.sub.3                                    H    S(O).sub.2 CH.sub.3                                                spiro-cyclopropyl     ______________________________________

                  TABLE 19     ______________________________________     R.sup.3 = ethyl, R.sup.1 = F, R.sup.4 = R.sup.5 = H,      ##STR34##     Formula R.sup.2      Formula X     ______________________________________     I       Cl           II      Direct bond     I       F            II      NCH.sub.3     I       NO.sub.2     II      NH     I       CF.sub.3     II      NCH.sub.2 CH.sub.3     ______________________________________

Formulation/Utility

Compounds of this invention will generally be used in formulation with an agriculturally suitable carrier comprising at least one of a liquid diluent, a solid diluent or a surfactant wherein the formulation is consistent with the physical properties of the active ingredient, mode of application and environmental factors such as soil type, moisture and temperature. Useful formulations include liquids such as solutions (including emulsifiable concentrates), suspensions, emulsions (including microemulsions and/or suspoemulsions) and the like which optionally can be thickened into gels. Useful formulations further include solids such as dusts, powders, granules, pellets, tablets, films, and the like which can be water-dispersible ("wettable") or water-soluble. Active ingredient can be (micro)encapsulated and further formed into a suspension or solid formulation; alternatively the entire formulation of active ingredient can be encapsulated (or "overcoated"). Encapsulation can control or delay release of the active ingredient. Sprayable formulations can be extended in suitable media and used at spray volumes from about one to several hundred liters per hectare. High-strength compositions are primarily used as intermediates for further formulation.

The formulations will typically contain effective amounts of active ingredient, diluent and surfactant within the following approximate ranges which add up to 100 percent by weight.

    ______________________________________                     Weight Percent                     Active                     Ingredient                            Diluent  Surfactant     ______________________________________     Water-Dispersible and Water-soluble                       5-90     0-94     1-15     Granules, Tablets and Powders.     Suspensions, Emulsions, Solutions                       5-50     40-95    0-15     (including Emulsifiable     Concentrates)     Dusts             1-25     70-99    0-5     Granules and Pellets                       0.01-99  5-99.99  0-15     High Strength Compositions                       90-99     0-10    0-2     ______________________________________

Typical solid diluents are described in Watkins, et al., Handbook of Insecticide Dust Diluents and Carriers, 2nd Ed., Dorland Books, Caldwell, New Jersey. Typical liquid diluents are described in Marsden, Solvents Guide, 2nd Ed., Interscience, New York, 1950. McCutcheon's Detergents and Emulsifiers Annual, Allured Publ. Corp., Ridgewood, N.J., as well as Sisely and Wood, Encyclopedia of Surface Active Agents, Chemical Publ. Co., Inc., New York, 1964, list surfactants and recommended uses. All formulations can contain minor amounts of additives to reduce foam, caking, corrosion, microbiological growth and the like, or thickeners to increase viscosity.

Surfactants include, for example, polyethoxylated alcohols, polyethoxylated alkylphenols, polyethoxylated sorbitan fatty acid esters, dialkyl sulfosuccinates, alkyl sulfates, alkylbenzene sulfonates, organosilicones, N,N-dialkyltaurates, lignin sulfonates, naphthalene sulfonate formaldehyde condensates, polycarboxylates, and polyoxyethylene/polyoxypropylene block copolymers. Solid diluents include, for example, clays such as bentonite, montmorillinite, attapulgite and kaolin, starch, sugar, silica, talc, diatomaceous earth, urea, calcium carbonate, sodium carbonate and bicarbonate, and sodium sulfate. Liquid diluents include, for example, water, N,N-dimethylformamide, dimethyl sulfoxide, N-alkylpyrrolidone, ethylene glycol, polypropylene glycol, paraffins, alkylbenzenes, alkylnaphthalenes, oils of olive, castor, linseed, tung, sesame, corn, peanut, cotton-seed, soybean, rape-seed and coconut, fatty acid esters, ketones such as cyclohexanone, 2-heptanone, isophorone and 4-hydroxy-4-methyl-2-pentanone, and alcohols such as methanol, cyclohexanol, decanol and tetrahydrofurfuryl alcohol.

Solutions, including emulsifiable concentrates, can be prepared by simply mixing the ingredients. Dusts and powders can be prepared by blending and, usually, grinding as in a hammer mill or fluid-energy mill. Suspensions are usually prepared by wet-milling; see, for example, U.S. Pat. No. 3,060,084. Granules and pellets can be prepared by spraying the active material upon preformed granular carriers or by agglomeration techniques. See Browning, "Agglomeration", Chemical Engineering, Dec. 4, 1967, pp 147-48, Perry's Chemical Engineer's Handbook, 4th Ed., McGraw-Hill, New York, 1963, pages 8-57 and following, and WO 91/13546. Pellets can be prepared as described in U.S. Pat. No. 4,172,714. Water-dispersible and water-soluble granules can be prepared as taught in U.S. Pat. No. 4,144,050, U.S. Pat. No.3,920,442 and U.S. Pat. No. DE 3,246,493. Tablets can be prepared as taught in U.S. Pat. No. 5,180,587, U.S. Pat. No. 5,232,701 and U.S. Pat. No. 5,208,030. Films can be prepared as taught in GB 2,095,558 and U.S. Pat. No. 3,299,566.

For further information regarding the art of formulation, see U.S. Pat. No. 3,235,361, Col. 6, line 16 through Col. 7, line 19 and Examples 10-41; U.S. Pat. No. 3,309,192, Col. 5, line 43 through Col. 7, line 62 and Examples 8, 12, 15, 39, 41, 52, 53, 58, 132, 138-140, 162-164, 166, 167 and 169-182; U.S. Pat. No. 2,891,855, Col. 3, line 66 through Col. 5, line 17 and Examples 1-4; Klingman, Weed Control as a Science, John Wiley and Sons, Inc., New York, 1961, pp 81-96; and Hance et al., Weed Control Handbook, 8th Ed., Blackwell Scientific Publications, Oxford, 1989.

In the following Examples, all percentages are by weight and all formulations are prepared in conventional ways. Compound numbers refer to compounds in Index Tables A-F.

    ______________________________________     Example A     ______________________________________     High Strength Concentrate     Compound 8                98.5%     silica aerogel            0.5%     synthetic amorphous fine silica                               1.0%     ______________________________________     Example B     ______________________________________     Wettable Powder     Compound 18               65.0%     dodecylphenol polyethylene glycol ether                               2.0%     sodium ligninsulfonate    4.0%     sodium silicoaluminate    6.0%     montmorillonite (calcined)                               23.0%     ______________________________________     Example C     ______________________________________     Granule     Compound 8                10.0%     attapulgite granules (low volatile                               90.0%     matter, 0.71/0.30 mm; U.S.S. No.     25-50 sieves)     ______________________________________     Example D     ______________________________________     Extruded Pellet     Compound 18               25.0%     anhydrous sodium sulfate  10.0%     crude calcium ligninsulfonate                               5.0%     sodium alkylnaphthalenesulfonate                               1.0%     calcium/magnesium bentonite                               59.0%     ______________________________________

Tests results indicate that the compounds of the present invention are highly active preemergent and/or postemergent herbicides and/or plant growth regulants. Many of them have utility for broad-spectrum pre- and/or postemergence weed control in areas where complete control of all vegetation is desired such as around fuel storage tanks, industrial storage areas, parking lots, drive-in theaters, around billboards and highway and railroad structures. Some of the compounds are useful for the control of selected grass and broadleaf weeds with tolerance to important agronomic crops which include but are not limited to barley, cotton, wheat, rape, sugarbeets, corn, soybeans, rice, and plantation crops including coffee, cocoa, oil palm, rubber, sugarcane, citrus, grapes, fruit trees, nut trees, banana, plantain, pineapple, conifers, e.g., loblolly pine, and turf species, e.g., Kentucky bluegrass, St. Augustine grass, Kentucky fescue and bermudagrass. Those skilled in the art will appreciate that not all compounds are equally effective against all weeds. Alternatively, the subject compounds are useful to modify plant growth.

Compounds of this invention can be used alone or in combination with other commercial herbicides, insecticides or fungicides. A mixture of one or more of the following herbicides with a compound of this invention may be particularly useful for weed control: acetochlor, acifluorfen and its sodium salt, acrolein (2-propenal), alachlor, arnetryn, amidosulfuron, amitrole, ammonium sulfamate, anilofos, asulam, atrazine, azimsulfuron, benazolin, benazolin-ethyl, benfluralin, benfuresate, bensulfuron-methyl, bensulide, bentazone, bifenox, bromacil, bromoxynil, bromoxynil octanoate, butachlor, butralin, butylate, chlomethoxyfen, chloramben, chlorbromuron, chloridazon, chlorimuron-ethyl, chlornitrofen, chlorotoluron, chlorpropham, chlorsulfuron, chlorthal-dimethyl, cinmethylin, cinosulfuron, clethodim, clomazone, clopyralid, clopyralid-olamine, cyanazine, cycloate, cyclosulfamuron, 2,4-D and its butotyl, butyl, isoctyl and isopropyl esters and its dimethylammonium, diolamine and trolamine salts, daimuron, dalapon, dalapon-sodium, dazomet, 2,4-DB and its dimethylammonium, potassium and sodium salts, desmedipham, desmetryn, dicamba and its dimethylammonium, potassium and sodium salts, dichlobenil, dichlorprop, diclofop-methyl, difenzoquat metilsulfate, diflufenican, dimepiperate, dimethylarsinic acid and its sodium salt, dinitramine, diphenamid, diquat dibromide, dithiopyr, diuron, DNOC, endothal, EPTC, esprocarb, ethalfluralin, ethametsulfuron-methyl, ethofumesate, ethyl α,2-dichloro-5- 4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl!-4-fluorobenzenepropanoate (F8426), fenoxaprop-ethyl, fenoxaprop-P-ethyl, fenuron, fenuron-TCA, flamprop-methyl, flamprop-M-isopropyl, flamprop-M-methyl, flazasulfuron, fluazifop-butyl, fluazifop-P-butyl, fluchloralin, flumetsulam, flumiclorac-pentyl, flumioxazin, fluometuron, fluoroglycofen-ethyl, flupoxam, fluridone, flurochloridone, fluroxypyr, fomesafen, fosamine-ammonium, glufosinate, glufosinate-ammonium, glyphosate, glyphosate-isopropylammonium, glyphosate-sesquisodium, glyphosate-trimesium, halosulfuron-methyl, haloxyfop-etotyl, haloxyfop-methyl, hexazinone, imazamethabenz-methyl, imazapyr, imazaquin, imazaquin-ammonium, imazethapyr, imazethapyr-ammonium, imazosulfuron, ioxynil, ioxynil octanoate, ioxynil-sodium, isoproturon, isouron, isoxaben, lactofen, lenacil, linuron, maleic hydrazide, MCPA and its dimethylammonium, potassium and sodium salts, MCPA-isoctyl, mecoprop, mecoprop-P, mefenacet, mefluidide, metam-sodium, methabenzthiazuron, methyl 2-chloro-4-fluoro-5- (tetrahydro-3-oxo-1H,3H- 1,3,4!thiadiazolo 3,4-.alpha.!pyridazin-1-ylidene)amino!phenyl!thioacetate (KIH 9201), methylarsonic acid and its calcium, monoammonium, monosodium and disodium salts, methyl 1- 5- 2-chloro-4-(trifluoromethyl)phenoxy!-2-nitrophenyl!-2-methoxethylidene!amino!oxy!acetate (AKH-7088), methyl 5- (4,6-dimethyl-2-pyrimidiny) amino!carbonyl!amino!sulfonyl!-1-(2-pyridinyl)-1H-pyrazole-4-carboxylate (NC-330), metobenzuron, metolachlor, metoxuron, metribuzin, metsulfuron-methyl, molinate, monolinuron, napropamide, naptalam, neburon, nicosulfuron, norflurazon, oryzalin, oxadiazon, oxyfluorfen, paraquat dichloride, pebulate, pendimethalin, perfluidone, phenmedipham, picloram, picloram-potassium, pretilachlor, primisulfuron-methyl, prometon, prometryn, propachlor, propanil, propazine, propham, propyza mnide, prosulfuron, pyrazolynate, pyrazosulfuron-ethyl, quinclorac, quizalofop-ethyl, quizalofop-P-ethyl, quizalofop-P-tefuryl, rimsulf uron, sethoxydim, siduron, simazine, sulcotrione (ICIA0051), sulfentrazone, sulfometuron-methyl, TCA, TCA-sodium, tebuthiuron, terbacil, terbuthylazine, terbutryn, thenylchlor, thifensulfuron-methyl, thiobencarb, tralkoxydim, tri-allate, triasulfuron, tribenuron-methyl, triclopyr, triclopyr-butotyl, triclopyr-triethylammonium, tridiphane, trifluralin, triflusulfuron-methyl, and vernolate.

In certain instances, combinations with other herbicides having a similar spectrum of control but a different mode of action will be particularly advantageous for preventing the development of resistant weeds.

Preferred are mixtures of a compound of Formula I with a compound selected from the group diuron, fluazifop-butyl, fluazifop-P-butyl, glufosinate, glufosinate-ammonium, glyphosate, glyphosate-isopropylammonium, glyphosate-sesquisodium, glyphosate-trimesium, hexazinone, metribuzin, norflurazon, paraquat, quizalofop-ethyl, and quizalofop-P-ethyl. Specifically preferred are mixtures of a compound selected from the group 3-(7-chloro-1-ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-yl)-1-methyl-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedione S,S-dioxide and 3- (7-chloro-1-ethyl-5-fluoro- 1,3-dihydro-2,1 -benzisothiazol-4-yl)imino!tetrahydro- 1H,3H- 1,3,4!thiadiazolo 3,4-α!pyridazin-1-one S,S-dioxide with a compound selected from the group diuron, fluazifop-butyl, fluazifop-P-butyl, glufosinate, glufosinate-ammonium, glyphosate, glyphosate-isopropyla rnmonium, glyphosate-sesquisodium, glyphosate-trimesium, hexazinone, metribuzin, norflurazon, paraquat, quizalofop-ethyl, and quizalofop-P-ethyl.

A herbicidally effective amount of the compounds of this invention is determined by a number of factors. These factors include: formulation selected, method of application, amount and type of vegetation present, growing conditions, etc. In general, a herbicidally effective amount of a compound(s) of this invention is applied at rates from about 0.001 to 20 kg/ha with a preferred rate range of 0.004 to 1.0 kg/ha. One skilled in the art can easily determine application rates necessary for the desired level of weed control.

The following Tests demonstrate the control efficacy of the compounds of this invention against specific weeds. The weed control afforded by the compounds is not limited, however, to these species. See Index Tables A-F for compound descriptions.

                  INDEX TABLE A     ______________________________________      ##STR35##     Cmpd No.            R.sup.1                  R.sup.2                        R.sup.3       R.sup.4                                          R.sup.5                                              m.p. (°C.)     ______________________________________     1 (Ex. 1)            F     H     CH.sub.2 CH.sub.3                                      H   H   189-190     2 (Ex. 2)            F     Cl    CH.sub.2 CH.sub.3                                      H   H   190-192     3 (Ex. 13)            F     Cl    CH.sub.2 -(4-CH.sub.3 OPh)                                      H   H   171-174     4 (Ex. 13)            F     Cl    H             H   H   75-79     5 (Ex. 14)            F     Cl    C(O)CH.sub.3  H   H   205-208     6.sup.a            F     Cl    CH.sub.2 CCH  H   H   solid*     ______________________________________      *See Index Table F for .sup.1 H NMR data.      .sup.a Compound contains 50% by weight of      2 1,3-bis(2-propynyl)-7-chloro-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-     l!-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione S,Sdioxide.

                                      INDEX TABLE B     __________________________________________________________________________      ##STR36##     Cmpd No.           R.sup.1              R.sup.2                R.sup.3  R.sup.4                            R.sup.5                              R.sup.13                                   R.sup.14                                      m.p. (°C.)     __________________________________________________________________________     7 (Ex. 4)           F  Cl                CH.sub.2 CH.sub.3                         H  H H    CF.sub.3                                      >230     8 (Ex. 5)           F  Cl                CH.sub.2 CH.sub.3                         H  H CH.sub.3                                   CF.sub.3                                      147-149     9 (Ex. 6)           F  Cl                CH.sub.2 CH.sub.3                         H  H CH.sub.2 CH.sub.3                                   CF.sub.3                                      177-178     10 (Ex. 15)           F  Cl                CH.sub.2 -(4-CH.sub.3 OPh)                         H  H H    CF.sub.3                                      >230     11 (Ex. 16)           F  Cl                CH.sub.2 -(4-CH.sub.3 OPh)                         H  H CH.sub.3                                   CF.sub.3                                      180-182     12 (Ex. 17)           F  Cl                H        H  H CH.sub.3                                   CF.sub.3                                      >230     13 (Ex. 18)           F  Cl                C(O)CH.sub.3                         H  H CH.sub.3                                   CF.sub.3                                      213-215     __________________________________________________________________________

                  INDEX TABLE C     ______________________________________      ##STR37##     Cmpd No.            R.sup.1                   R.sup.2                         R.sup.3 R.sup.4                                      R.sup.5                                           Z.sup.1                                                m.p. (°C.)     ______________________________________     14 (Ex. 8)            F      Cl    CH.sub.2 CH.sub.3                                 H    H    CH.sub.2                                                168-169     15 (Ex. 9)            F      Cl    CH.sub.2 CH.sub.3                                 H    H    O    200-202     ______________________________________

                                      INDEX TABLE D     __________________________________________________________________________      ##STR38##     Cmpd No.           R.sup.1              R.sup.2                 R.sup.3                      R.sup.4                         R.sup.5                            J          m.p. (°C.)     __________________________________________________________________________     16 (Ex. 10)           F  Cl CH.sub.2 CH.sub.3                      H  H                             ##STR39## oil*     17 (Ex. 11)           F  Cl CH.sub.2 CH.sub.3                      H  H                             ##STR40## 87-90     18 (Ex. 7)           F  Cl CH.sub.2 CH.sub.3                      H  H                             ##STR41## 143-146     19 (Ex. 12)           F  Cl CH.sub.2 CH.sub.3                      H  H                             ##STR42## semisolid*     __________________________________________________________________________      *See Index Table F for .sup.1 H NMR data.

                  INDEX TABLE E     ______________________________________      ##STR43##     Cmpd No.             R.sup.1                    R.sup.3  R.sup.4                                  R.sup.5                                      X       m.p. (°C.)     ______________________________________     20 (Ex. 19)             F      CH.sub.2 Ph                             H    H   O       150-152     21 (Ex. 3)             F      CH.sub.2 CH.sub.3                             H    H   direct bond                                              oil*     ______________________________________      *See Index Table F for .sup.1 H NMR data.

                  INDEX TABLE F     ______________________________________     Cmpd No.            .sup.1 H NMR data (in CDCl.sub.3 solution unless otherwise            indicated).sup.a     ______________________________________      6     δ 7.26 (d,1H), 4.58 (s,2H), 4.48 (m,2H), 2.42 (br s,4H),            2.21            (t,1H), 1.82 (br s,2H).     16     δ 7.30 (d,1H,J = 9.6 Hz), 5.99 (s,2H), 4.31 (s,2H), 4.21            (s,4H), 3.93 (dd,2H), 1.28 (t,3H).     19     δ 7.26 (d,1H), 7.04 t,1H), 4.28 (s,2H), 3.96 (q,2H), 2.44            (s,3H), 1.26 (t,3H).     21     δ 7.08 (d,1H), 6.62 (d,2H), 4.32 (s,2H), 3.64 (q,2H), 2.42            (m,4H), 1.82 (m,4H), 1.38 (t,3H).     ______________________________________      .sup.a1 H NMR data are in ppm downfield from tetramethylsilane. Couplings      are designated by (s)singlet, (d)doublet, (t)triplet, (q)quartlet,      (m)multiplet, (dd)doublet of doublets, (br s)broad singlet.

Seeds of barley (Hordeum vulgare), bamyardgrass (Echinochloa crus-galli), bedstraw (Galium aparine), blackgrass (Alopecurus myosuroides), chickweed (Stellaria media), cocklebur (Xanthium pensylvanicum), corn (Zea mays), cotton (Gossypium hirsutum), crabgrass (Digitaria sanguinalis), downy brome (Bromus tectorum), giant foxtail (Setaria faberii), lambsquarters (Chenopodium album), morningglory (Ipomoea hederacea), rape (Brassica napus), rice (Oryza sativa), sorghum (Sorghum bicolor), soybean (Glycine max), sugar beet (Beta vulgaris), velvetleaf (Abutilon theophrasti), wheat (Triticum aestivum), wild buckwheat (Polygonum convolvulus), wild oat (Avena fatua) and purple nutsedge (Cyperus rotundus) tubers were planted and treated preemergence with test chemicals formulated in a non-phytotoxic solvent mixture which includes a surfactant.

At the same time, these crop and weed species were also treated with postemergence applications of test chemicals formulated in the same manner. Plants ranged in height from two to eighteen cm (one to four leaf stage) for postemergence treatments. Treated plants and controls were maintained in a greenhouse for twelve to sixteen days, after which all species were compared to controls and visually evaluated. Plant response ratings, summarized in Table A, are based on a scale of 0 to 10 where 0 is no effect and 10 is complete control. A dash (-) response means no test result.

    __________________________________________________________________________     TABLE A     COMPOUND   TABLE A     COMPOUND     __________________________________________________________________________     Rate 2000 g/ha                 7          Rate 2000 g/ha                                        7     POSTEMERGENCE          PREEMERGENCE     Barley      0          Barley      0     Barnyardgrass                 0          Barnyardgrass                                        0     Bedstraw    2          Bedstraw    0     Blackgrass  1          Blackgrass  0     Chickweed   0          Chickweed   0     Cocklebur   2          Cocklebur   0     Corn        1          Corn        0     Cotton      2          Cotton      0     Crabgrass   1          Crabgrass   0     Downy brome 0          Downy brome 0     Giant foxtail                 1          Giant foxtail                                        0     Lambsquarter                 1          Lambsquarter                                        0     Morningglory                 2          Morningglory                                        3     Nutsedge    0          Nutsedge    0     Rape        2          Rape        0     Rice        0          Rice        0     Sorghum     0          Sorghum     0     Soybean     2          Soybean     2     Sugar beet  1          Sugar beet  0     Velvetleaf  1          Velvetleaf  0     Wheat       0          Wheat       0     Wild buckwheat                 2          Wild buckwheat                                        0     Wild oat    0     __________________________________________________________________________     TABLE A   COMPOUND     TABLE A   COMPOUND     __________________________________________________________________________     Rate 1000 g/ha               1   2  16 20 Rate 1000 g/ha                                      1   2  16 20     POSTEMERGENCE          PREEMERGENCE     Barley    3   4  3  3  Barley    0   0  0  0     Barnyardgrass               3   9  6  6  Barnyardgrass                                      6   9  8  0     Bedstraw  7   10 6  6  Bedstraw  8   10 10 --     Blackgrass               4   5  3  2  Blackgrass                                      3   3  2  2     Chickweed 3   8  5  2  Chickweed 3   9  2  --     Cocklebur 6   9  8  8  Cocklebur 0   4  8  3     Corn      3   5  2  2  Corn      2   3  3  2     Cotton    9   10 10 9  Cotton    0   10 10 0     Crabgrass 3   6  5  7  Crabgrass 4   9  8  3     Downy brome               3   2  2  2  Downy brome                                      2   3  0  --     Giant foxtail               3   6  7  4  Giant foxtail                                      2   8  9  4     Lambsquarter               8   9  9  8  Lambsquarter                                      9   10 10 --     Morningglory               9   9  9  8  Morningglory                                      1   10 8  4     Nutsedge  0   2  2  2  Nutsedge  0   5  -- --     Rape      7   10 10 7  Rape      6   10 10 --     Rice      5   6  7  5  Rice      0   4  3  0     Sorghum   3   8  6  2  Sorghum   0   2  7  0     Soybean   5   8  9  5  Soybean   0   7  8  0     Sugar beet               9   10 10 4  Sugar beet                                      8   10 10 --     Velvetleaf               8   10 10 6  Velvetleaf                                      8   10 10 2     Wheat     4   4  3  2  Wheat     0   2  3  0     Wild buckwheat               10  10 9  6  Wild buckwheat                                      0   10 9  --     Wild oat  3   4  2  2  Wild oat  2   4  2  0     __________________________________________________________________________     TABLE A    COMPOUND    TABLE A    COMPOUND     __________________________________________________________________________     Rate 400 g/ha                7     12    Rate 400 g/ha                                       7     12     POSTEMERGENCE          PREEMERGENCE     Barley     0     10    Barley     0     0     Barnyardgrass                1     10    Barnyardgrass                                       0     3     Bedstraw   1     10    Bedstraw   0     10     Blackgrass 0     6     Blackgrass 0     2     Chickweed  0     10    Chickweed  0     2     Cocklebur  1     10    Cocklebur  0     10     Corn       0     10    Corn       0     0     Cotton     --    10    Cotton     0     10     Crabgrass  0     8     Crabgrass  0     4     Downy brome                0     8     Downy brome                                       0     3     Giant foxtail                0     9     Giant foxtail                                       0     5     Lambsquarter                0     10    Lambsquarter                                       0     9     Morningglory                --    10    Morningglory                                       1     10     Nutsedge   0     5     Nutsedge   0     7     Rape       0     10    Rape       0     9     Rice       0     10    Rice       0     5     Sorghum    0     10    Sorghum    0     0     Soybean    1     10    Soybean    0     9     Sugar beet 1     10    Sugar beet 0     10     Velvetleaf 1     10    Velvetleaf 0     10     Wheat      0     10    Wheat      0     0     Wild buckwheat                1     10    Wild buckwheat                                       0     6     Wild oat   0     10    Wild oat   0     0     __________________________________________________________________________     TABLE A   COMPOUND     __________________________________________________________________________     Rate 200 g/ha               1 2 3 4 5 6 8 9 10                                 11                                   13                                     14                                       15                                         16                                           17                                             18                                               20                                                 21     POSTEMERGENCE     Barley    3 3 5 2 3 5 8 6 0 4 6 2 1 3 5 9 3 2     Barnyardgrass               2 7 4 10                       10                         7 10                             10                               0 6 10                                     3 7 2 9 9 6 5     Bedstraw  5 10                   4 8 9 9 10                             10                               0 10                                   10                                     5 6 5 10                                             10                                               5 6     Blackgrass               3 3 2 2 6 3 7 9 0 3 2 3 2 2 3 6 1 1     Chickweed 3 4 2 6 9 4 10                             3 0 7 10                                     3 6 3 3 8 1 3     Cocklebur 6 9 10                     10                       10                         10                           10                             3 0 10                                   10                                     7 6 7 8 10                                               7 7     Corn      2 3 3 6 2 3 9 9 0 2 9 1 4 1 3 5 2 2     Cotton    9 10                   --                     10                       10                         10                           10                             9 0 10                                   10                                     10                                       10                                         9 10                                             10                                               10                                                 9     Crabgrass 2 4 5 6 4 4 9 2 0 2 6 2 2 2 5 9 4 5     Downy brome               2 3 2 2 2 1 7 5 0 2 2 1 0 1 3 5 2 1     Giant foxtail               2 4 6 5 5 4 9 6 0 2 6 2 3 2 6 9 3 3     Lambsquarter               8 9 10                     10                       9 10                           10                             9 0 10                                   10                                     8 8 8 9 10                                               9 8     Morningglory               8 9 10                     10                       10                         10                           10                             8 0 10                                   10                                     9 9 9 10                                             10                                               9 9     Nutsedge  0 2 1 4 2 2 5 --                               0 0 3 2 --                                         1 8 --                                               1 3     Rape      3 10                   10                     10                       10                         10                           10                             9 0 10                                   10                                     5 8 7 10                                             10                                               6 6     Rice      3 6 4 5 6 4 10                             3 0 3 10                                     4 4 3 5 7 3 5     Sorghum   3 3 4 4 6 4 10                             9 0 5 9 2 3 3 6 8 2 4     Soybean   3 8 5 5 5 5 10                             9 0 8 10                                     8 9 8 9 10                                               3 7     Sugar beet               8 10                   10                     10                       10                         10                           10                             10                               0 10                                   10                                     9 10                                         9 10                                             10                                               5 10     Velvetleaf               6 10                   10                     10                       10                         10                           10                             10                               0 10                                   10                                     10                                       10                                         10                                           10                                             10                                               7 9     Wheat     3 4 3 3 4 3 10                             9 0 3 6 4 3 2 2 9 2 1     Wild buckwheat               8 10                   10                     10                       10                         10                           10                             10                               0 10                                   10                                     7 10                                         8 10                                             10                                               3 8     Wild oat  2 3 2 2 3 2 9 9 0 3 3 4 4 1 2 7 2 1     __________________________________________________________________________     TABLE A   COMPOUND     __________________________________________________________________________     Rate 200 g/ha               1 2 3 4 5 6 8 9 10                                 11                                   13                                     14                                       15                                         16                                           17                                             18                                               20                                                 21     PREEMERGENCE     Barley    0 0 0 0 0 0 6 2 0 0 0 0 0 2 0 3 0 0     Barnyardgrass               0 9 0 0 2 4 10                             9 0 2 0 3 2 3 7 9 0 5     Bedstraw  2 10                   8 0 3 2 10                             10                               0 10                                   10                                     7 3 2 10                                             6 0 9     Blackgrass               2 3 1 0 0 0 9 0 0 0 0 3 1 1 0 5 0 2     Chickweed 0 7 0 0 0 0 10                             8 0 0 0 3 4 0 0 3 0 0     Cocklebur 0 3 7 4 2 7 10                             1 0 3 10                                     3 3 6 4 6 2 0     Corn      0 0 0 0 0 2 7 1 0 0 0 2 3 0 3 2 0 0     Cotton    0 0 0 0 0 0 10                             7 0 0 9 6 6 7 10                                             3 0 3     Crabgrass 0 8 3 0 0 2 10                             10                               0 9 6 8 2 2 7 6 2 2     Downy brome               3 2 1 0 0 0 10                             0 0 2 0 0 0 0 2 4 0 1     Giant foxtail               0 6 0 0 0 3 10                             10                               0 9 0 6 6 4 9 9 0 0     Lambsquarter               5 10                   10                     10                       10                         10                           10                             10                               0 10                                   9 10                                       10                                         10                                           10                                             10                                               --                                                 10     Morningglory               0 10                   0 0 6 9 10                             1 0 10                                   10                                     3 4 8 10                                             7 0 0     Nutsedge  0 0 --                     0 0 --                           6 0 --                                 0 0 --                                       --                                         0 1 0 0 0     Rape      3 9 0 0 7 0 10                             9 0 2 8 4 7 9 10                                             7 0 8     Rice      0 0 0 0 0 0 9 0 0 0 3 1 3 1 4 2 0 0     Sorghum   0 0 0 0 0 0 10                             8 0 0 0 2 1 0 7 2 0 0     Soybean   0 5 2 0 0 0 10                             2 0 0 10                                     1 3 7 7 7 0 0     Sugar beet               0 10                   8 2 7 8 10                             10                               0 10                                   10                                     10                                       10                                         7 10                                             10                                               2 10     Velvetleaf               2 10                   7 3 8 6 10                             10                               0 10                                   10                                     8 10                                         10                                           10                                             10                                               0 0     Wheat     0 2 0 0 0 0 9 5 0 1 2 3 0 0 0 6 0 0     Wild buckwheat               0 9 0 0 2 0 10                             9 0 0 3 0 3 0 10                                             5 --                                                 2     Wild oat  2 2 0 0 0 0 8 1 0 1 3 3 0 2 3 6 0 0     __________________________________________________________________________     TABLE A     COMPOUND   TABLE A     COMPOUND     __________________________________________________________________________     Rate 100 g/ha                 12         Rate 100 g/ha                                        12     POSTEMERGENCE          PREEMERGENCE     Barley      8          Barley      0     Barnyardgrass                 10         Barnyardgrass                                        0     Bedstraw    10         Bedstraw    6     Blackgrass  3          Blackgrass  0     Chickweed   10         Chickweed   0     Cocklebur   10         Cocklebur   6     Corn        8          Corn        0     Cotton      10         Cotton      0     Crabgrass   7          Crabgrass   0     Downy brome 5          Downy brome 0     Giant foxtail                 6          Giant foxtail                                        0     Lambsquarter                 10         Lambsquarter                                        6     Morningglory                 10         Morningglory                                        10     Nutsedge    3          Nutsedge    3     Rape        10         Rape        6     Rice        10         Rice        2     Sorghum     10         Sorghum     0     Soybean     8          Soybean     8     Sugar beet  10         Sugar beet  8     Velvetleaf  10         Velvetleaf  3     Wheat       10         Wheat       0     Wild buckwheat                 10         Wild buckwheat                                        0     Wild oat    9          Wild oat    0     __________________________________________________________________________     TABLE A   COMPOUND     __________________________________________________________________________     Rate 50 g/ha               3  4 5 6 8  9 10 11                                  13 14                                       15 17                                            18                                              19                                                21     POSTEMERGENCE     Barley    3  2 3 4 3  4 0  3 7  0 0  3 5 3 2     Barnyardgrass               3  6 10                      6 10 9 0  2 10 1 2  6 9 4 3     Bedstraw  4  7 9 9 10 9 0  10                                  10 3 6  9 8 6 3     Blackgrass               2  1 3 2 7  8 0  3 2  2 1  0 6 3 1     Chickweed 2  4 6 2 10 3 0  7 10 2 1  2 8 8 2     Cocklebur 10 9 10                      10                        10 2 0  10                                  10 7 3  7 10                                              7 5     Corn      3  3 2 3 9  5 0  2 9  1 2  3 2 3 2     Cotton    10 10                    10                      10                        10 9 0  10                                  10 10                                       10 10                                            10                                              10                                                9     Crabgrass 3  3 4 4 6  3 0  2 6  2 2  3 4 3 4     Downy brome               1  1 2 1 6  4 0  1 3  1 1  2 5 3 1     Giant foxtail               4  3 6 3 6  5 0  2 6  2 2  6 8 3 3     Lambsquarter               9  8 9 9 10 8 0  10                                  10 8 9  9 9 10                                                6     Morningglory               9  10                    10                      10                        10 5 0  10                                  10 9 7  10                                            10                                              9 4     Nutsedge  1  1 --                      2 3  --                             0  0 3  --                                       1  7 2 1 1     Rape      9  10                    10                      10                        10 9 0  10                                  10 3 5  9 9 3 3     Rice      3  3 4 3 9  2 0  3 10 3 3  5 4 3 4     Sorghum   3  3 6 4 6  4 0  2 10 2 2  4 7 5 4     Soybean   2  3 4 2 10 9 0  8 9  8 7  9 7 3 5     Sugar beet               10 10                    10                      10                        10 6 0  10                                  10 7 9  10                                            10                                              10                                                9     Velvetleaf               10 10                    10                      10                        10 9 0  10                                  10 10                                       6  10                                            10                                              9 6     Wheat     3  3 4 2 10 7 0  2 9  1 2  2 7 3 1     Wild buckwheat               10 10                    10                      10                        10 9 0  10                                  10 7 9  9 10                                              10                                                6     Wild oat  1  2 3 2 5  9 0  2 6  3 3  1 6 2 1     __________________________________________________________________________     TABLE A   COMPOUND     __________________________________________________________________________     Rate 50 g/ha               3  4 5 6 8  9 10 11                                  13 14                                       15 17                                            18                                              19                                                21     PREEMERGENCE     Barley    0  0 0 0 3  0 0  0 0  0 0  0 3 0 0     Barnyardgrass               0  0 0 0 10 1 0  0 0  0 0  4 6 3 1     Bedstraw  0  0 2 0 10 9 0  10                                  10 0 0  10                                            3 0 0     Blackgrass               0  0 0 0 3  0 0  0 0  2 0  0 0 0 0     Chickweed 0  0 0 0 10 1 0  0 0  0 0  0 0 0 0     Cocklebur 3  0 0 0 9  0 0  2 0  2 0  4 2 0 0     Corn      0  0 0 0 5  0 0  0 0  0 0  2 0 3 0     Cotton    0  0 0 0 10 2 0  0 1  0 3  9 0 10                                                0     Crabgrass 0  0 0 0 8  9 0  3 0  0 0  2 0 0 0     Downy brome               0  0 0 0 7  0 0  0 0  2 0  0 3 1 2     Giant foxtail               0  0 0 0 10 8 0  4 0  0 0  7 2 3 0     Lambsquarter               3  5 9 8 10 9 0  10                                  7  10                                       9  8 9 7 9     Morningglory               0  0 3 0 10 0 0  10                                  10 0 0  3 2 0 0     Nutsedge  -- --                    0 0 1  0 -- --                                  0  --                                       -- 0 0 0 0     Rape      0  0 0 0 10 4 0  --                                  2  0 0  10                                            1 0 0     Rice      0  0 0 0 5  0 0  0 0  0 0  1 0 0 0     Sorghum   0  0 0 0 4  0 0  0 0  0 0  3 0 0 0     Soybean   0  0 0 0 9  0 0  0 0  0 0  7 0 3 0     Sugar beet               0  2 3 7 10 5 0  8 7  7 9  9 9 9 9     Velvetleaf               0  0 2 3 10 1 0  10                                  2  6 2  10                                            6 5 0     Wheat     0  0 0 0 5  2 0  1 0  0 0  0 2 1 0     Wild buckwheat               0  0 0 0 10 4 0  0 0  0 0  8 0 0 0     Wild oat  0  0 0 0 3  2 0  0 0  0 0  0 3 1 0     __________________________________________________________________________     TABLE A     COMPOUND   TABLE A     COMPOUND     __________________________________________________________________________     Rate 10 g/ha                 19         Rate 10 g/ha                                        19     POSTEMERGENCE          PREEMERGENCE     Barley      2          Barley      0     Barnyardgrass                 3          Barnyardgrass                                        3     Bedstraw    3          Bedstraw    0     Blackgrass  1          Blackgrass  0     Chickweed   3          Chickweed   0     Cocklebur   4          Cocklebur   0     Corn        2          Corn        0     Cotton      --         Cotton      5     Crabgrass   3          Crabgrass   0     Downy brome 1          Downy brome 0     Giant foxtail                 2          Giant foxtail                                        0     Lambsquarter                 6          Lambsquarter                                        4     Morningglory                 6          Morningglory                                        0     Nutsedge    1          Nutsedge    0     Rape        1          Rape        0     Rice        2          Rice        2     Sorghum     3          Sorghum     0     Soybean     3          Soybean     3     Sugar beet  10         Sugar beet  1     Velvetleaf  8          Velvetleaf  3     Wheat       3          Wheat       0     Wild buckwheat                 10         Wild buckwheat                                        0     Wild oat    1          Wild oat    0     __________________________________________________________________________

Test B

The compounds evaluated in this test were formulated in a non-phytotoxic solvent mixture which includes a surfactant and applied to the soil surface before plant seedlings emerged (preemergence application), to water that covered the soil surface (flood application), and to plants that were in the one-to-four leaf stage (postemergence application). A sandy loam soil was used for the preemergence and postemergence tests, while a silt loam soil was used in the flood test. Water depth was approximately 2.5 cm for the flood test and was maintained at this level for the duration of the test.

Plant species in the preemergence and postemergence tests consisted of barnyardgrass (Echinochloa crus-galli), barley (Hordeum vulgare), bedstraw (Galium aparine), blackgrass (Alopecurus myosuroides), chickweed (Stellaria media), cocklebur (Xanthium pensylvanicum), corn (Zea mays), cotton (Gossypium hirsutum), crabgrass (Digitaria sanguinalis), downy brome (Bromus tectorum), giant foxtail (Setaria faberii), johnsongrass (Sorghum halpense), lambsquarters (Chenopodium album), morningglory (Ipomoea hederacea), pigweed (Amaranthus retroflexus), rape (Brassica napus), ryegrass (Lolium multiflorum), soybean (Glycine max), speedwell (Veronica persica), sugar beet (Beta vulgaris), velvetleaf (Abutilon theophrasti), wheat (Triticum aestivum), wild buckwheat (Polygonum convolvulus), and wild oat (Avenafatua). All plant species were planted one day before application of the compound for the preemergence portion of this test. Plantings of these species were adjusted to produce plants of appropriate size for the postemergence portion of the test. Plant species in the flood test consisted of rice (Oryza sativa), umbrella sedge (Cyperus difformis), duck salad (Heteranthera limosa), barnyardgrass (Echinochloa crus-galli) and late watergrass (Echinochloa oryzicola) grown to the 2 leaf stage for testing.

All plant species were grown using normal greenhouse practices. Visual evaluations of injury expressed on treated plants, when compared to untreated controls, were recorded approximately fourteen to twenty one days after application of the test compound. Plant response this ratings, summarized in Table B, were recorded on a 0 to 100 scale where 0 is no effect and 100 is complete control. A dash (-) response means no test result.

                                      TABLE B     __________________________________________________________________________                COMPOUND          COMPOUND     Rate 500 g/ha                 2       Rate 250 g/ha                                  2    9  14     __________________________________________________________________________     POST-               POST-     EMERGENCE           EMERGENCE     Barley Igri                --       Barley Igri                                  35   65 30     Barnyardgr. (Flood)                70       Barnyardgr. (Flood)                                  35   95 25     Barnyardgrass                --       Barnyardgrass                                  45   100                                          40     Bedstraw   --       Bedstraw 85   100                                          35     Blackgrass --       Blackgrass                                  10   90 40     Chickweed  --       Chickweed                                  30   70 70     Cocklebur  --       Cocklebur                                  90   75 80     Corn       --       Corn     25   90 40     Cotton     --       Cotton   100  100                                          100     Crabgrass  --       Crabgrass                                  25   70 55     Downy Brome                --       Downy Brome                                  0    35 40     Duck salad 25       Duck salad                                  20   0  95     Giant foxtail                --       Giant foxtail                                  40   90 50     Italn. Rygrass                --       Italn. Rygrass                                  0    30 35     Johnsongrass                --       Johnsongrass                                  50   90 75     Lambsquarter                --       Lambsquarter                                  100  100                                          95     Morningglory                --       Morningglory                                  100  90 100     Rape       --       Rape     100  100                                          90     Redroot Pigweed                --       Redroot Pigweed                                  --   100                                          90     Rice Japonica                60       Rice Japonica                                  45   75 70     Soybean    --       Soybean  --   60 60     Speedwell  --       Speedwell                                  100  -- 100     Sugar beet --       Sugar beet                                  100  100                                          100     Umbrella sedge                65       Umbrella sedge                                  45   60 100     Velvetleaf --       Velvetleaf                                  100  100                                          100     Watergrass 75       Watergrass                                  35   80 30     Wheat      --       Wheat    30   60 30     Wild buckwheat                --       Wild buckwheat                                  65   100                                          100     Wild oat   --       Wild oat 35   90 40              COMPOUND           COMPOUND     Rate 250 g/ha              2  9   14 Rate 125 g/ha                                 2  9   14 17     __________________________________________________________________________     PREEMERGENCE       POST-                        EMERGENCE     Barley Igri              10 10  0  Barley Igri                                 35 35  30 25     Barnyardgrass              40 100 90 Barnyardgr. (Flood)                                 10 65  0  75     Bedstraw 20 100 85 Barnyardgrass                                 35 100 35 75     Blackgrass              0  65  45 Bedstraw 60 100 35 100     Chickweed              10 30  10 Blackgrass                                 10 80  35 30     Cocklebur              0  10  85 Chickweed                                 30 50  70 60     Corn     10 40  25 Cocklebur                                 90 50  80 95     Cotton   40 80  95 Corn     15 90  30 30     Crabgrass              75 95  85 Cotton   100                                    100 100                                           100     Downy Brome              0  0   0  Crabgrass                                 20 60  45 30     Giant foxtail              85 100 90 Downy Brome                                 0  25  20 20     Italn. Rygrass              0  90  75 Duck salad                                 0  0   80 95     Johnsongrass              90 100 45 Giant foxtail                                 40 85  30 50     Lambsquarter              95 100 100                        Italn. Rygrass                                 0  20  20 30     Morningglory              100                 60  25 Johnsongrass                                 40 90  40 75     Rape     30 95  85 Lambsquarter                                 85 100 65 100     Redroot Pigweed              100                 100 90 Morningglory                                 100                                    80  90 100     Soybean  10 50  30 Rape     100                                    100 90 100     Speedwell              -- 100 100                        Redroot Pigweed                                 100                                    100 90 90     Sugar beet              95 100 100                        Rice Japonica                                 30 45  45 75     Velvetleaf              100                 100 100                        Soybean  100                                    40  50 85     Wheat    0  35  10 Speedwell                                 100                                    --  100                                           100     Wild buckwheat              0  100 85 Sugar beet                                 100                                    100 100                                           100     Wild oat 35 95  30 Umbrella sedge                                 15 0   95 85                        Velvetleaf                                 100                                    100 100                                           100                        Watergrass                                 10 35  25 70                        Wheat    25 45  20 30                        Wild buckwheat                                 65 100 80 100                        Wild oat 35 90  35 35                      COMPOUND     Rate 125 g/ha    2  9        14 17     __________________________________________________________________________     PREEMERGENCE     Barley Igri      0  10       0 20     Barnyardgrass    20 85       10 70     Bedstraw         0  100      0  100     Blackgrass       0  50       45 0     Chickweed        10 10       0  0     Cocklebur        0  0        35 70     Corn             0  25       0  20     Cotton           0  70       50 100     Crabgrass        20 75       20 65     Downy Brome      0  0        0  10     Giant foxtail    50 100      20 55     Italn. Rygrass   0  20       0  0     Johnsongrass     30 50       30 50     Lambsquarter     95 100      95 100     Morningglory     0  50       20 80     Rape             0  75       10 100     Redroot Pigweed  100                         100      10 100     Soybean          0  30       10 50     Speedwell        -- 100      0  100     sugar beet       30 100      0  100     Velvetleaf       100                         100      10 100     Wheat            0  20       0  0     Wild buckwheat   0  90       35 100     Wild oat         25 85       0  20               COMPOUND     Rate 62 g/ha               2   3   4   6   8   9   14  17     __________________________________________________________________________     POSTEMERGENCE     Barley Igri               35  35  30  30  35  30  30  25     Barnyardgr. (Flood)               10  30  25  25  100 10  0   60     Barnyardgrass               35  25  70  30  100 95  30  60     Bedstraw  60  70  100 100 100 95  0   100     Blackgrass               10  20  25  45  55  80  30  25     Chickweed 30  40  75  70  100 50  55  60     Cocklebur 90  90  100 100 100 40  70  90     Corn      10  40  35  50  90  70  25  30     Cotton    100 100 100 100 100 100 100 100     Crabgrass 15  50  40  40  70  50  35  30     Downy Brome               0   15  20  30  10  10  20  0     Duck salad               0   0   0   0   0   0   0   80     Giant foxtail               35  60  50  60  90  70  20  30     Italn. Rygrass               0   0   15  20  75  0   10  25     Johnsongrass               30  40  70  70  100 90  30  60     Lambsquarter               85  95  85  100 100 95  65  100     Morningglory               100 100 100 100 100 60  90  95     Rape      60  100 100 --  100 100 90  100     Redroot Pigweed               95  100 100 100 100 100 75  70     Rice Japonica               20  30  25  25  80  35  0   45     Soybean   70  50  50  50  --  40  --  80     Speedwell 100 90  95  100 100 --  80  100     sugar beet               100 100 100 100 100 100 60  100     Umbrella sedge               10  0   0   0   0   0   80  75     Velvetleaf               100 100 100 100 100 100 100 100     Watergrass               0   20  15  15  100 35  0   65     Wheat     25  35  10  15  40  40  10  0     Wild buckwheat               65  100 100 95  100 100 35  100     Wild oat  35  25  20  25  30  65  20  30     Rate 62 g/ha     __________________________________________________________________________     PREEMERGENCE     Barley Igri               0   0   0   0   0   10  0   10     Barnyardgrass               10  20  0   30  100 35  0   20     Bedstraw  0   25  10  0   100 85  0   95     Blackgrass               0   0   0   10  20  10  20  0     Chickweed 10  20  10  100 10  0   0     Cocklebur 0   0   0   55  50  0   20  50     Corn      0   0   0   0   40  0   0   0     Cotton    0   0   0   0   100 50  20  100     Crabgrass 0   0   0   0   95  35  15  40     Downy Brome               0   0   0   0   10  0   0   0     Giant foxtail               20  0   0   0   100 90  --  30     Italn. Rygrass               0   0   0   0   50  10  0   0     Johnsongrass               10  0   0   20  95  30  0   30     Lambsquarter               40  90  85  95  100 100 0   100     Morningglory               0   15  10  35  100 50  10  70     Rape      0   0   0   0   100 65  0   80     Redroot Pigweed               100 0   0   10  100 100 --  80     Soybean   0   10  10  0   100 20  0   35     Speedwell --  10  50  25  100 100 0   85     Sugar beet               10  0   10  25  100 100 0   100     Velvetleaf               100 60  10  85  100 30  0   100     Wheat     0   0   0   0   10  10  0   0     Wild buckwheat               0   25  10  0   100 60  0   95     Wild oat  10  0   0   0   50  20  0   0     Rate 31 g/ha     __________________________________________________________________________     POSTEMERGENCE     Barley Igri               30  35  --  30  35  20  20  20     Barnyardgr. (Flood)               --  30  20  25  75  0   0   20     Barnyardgrass               30  20  60  25  100 95  --  30     Bedstraw  50  70  90  100 100 90  0   65     Blackgrass               10  20  25  40  40  60  20  20     Chickweed 30  40  70  65  100 50  50  50     Cocklebur 35  90  100 100 100 40  70  70     Corn      10  30  30  30  90  55  --  20     Cotton    100 100 100 100 100 100 90  100     Crabgrass 10  40  30  40  50  35  35  20     Downy Brome               0   15  20  30  0   0   0   0     Duck salad               --  0   0   0   0   0   0   45     Giant foxtail               30  35  40  50  85  40  20  30     Italn. Rygrass               0   0   15  20  45  0   10  0     Johnsongrass               20  30  40  --  90  80  --  30     Lambsquarter               80  95  75  100 100 90  65  76     Morningglory               80  100 100 100 100 60  60  90     Rape      60  90  95  --  100 95  75  100     Redroot Pigweed               95  90  90  90  100 100 70  70     Rice Japonica               --  25  25  25  70  15  0   35     Soybean   70  50  40  50  100 40  50  70     Speedwell 100 70  --  95  100 --  80  85     Sugar beet               80  100 100 100 100 95  40  100     Umbrella sedge               --  0   0   0   0   0   35  45     Velvetleaf               100 100 100 100 100 100 90  100     Watergrass               --  20  15  10  60  20  0   20     Wheat     25  30  10  15  40  35  0   0     Wild buckwheat               65  95  100 95  100 100 35  95     Wild oat  35  25  20  25  30  40  20  25     Rate 31 g/ha     __________________________________________________________________________     PREEMERGENCE     Barley Igri               0   0   0   0   0   0   0   0     Barnyardgrass               0   20  0   20  95  10  0   10     Bedstraw  0   0   10  0   100 40  0   30     Blackgrass               0   0   0   0   10  0   0   0     Chickweed --  0   20  10  85  0   0   0     Cocklebur 0   0   0   20  30  0   10  40     Corn      0   0   0   0   30  0   0   0     Cotton    0   0   0   0   100 10  0   100     Crabgrass 0   0   0   0   75  0   0   10     Downy Brome               0   0   0   0   0   0   0   0     Giant foxtail               0   0   0   0   100 15  0   0     Italn. Rygrass               0   0   0   6   35  0   0   0     Johnsongrass               0   0   0   10  35  10  0   0     Lambsquarter               20  85  85  95  100 100 0   70     Morningglory               0   0   10  30  30  10  0   35     Rape      0   0   0   0   75  0   0   40     Redroot Pigweed               90  0   0   10  100 100 0   70     Soybean   0   10  0   0   50  20  0   20     Speedwell --  0   50  25  100 10  0   10     Sugar beet               0   0   0   0   85  50  0   90     Velvetleaf               0   0   10  30  100 0   0   100     Wheat     0   0   0   0   0   0   0   0     Wild buckwheat               0   0   0   0   100 0   0   90     Wild oat  0   0   0   0   30  20  0   0                 COMPOUND     Rate 16 g/ha                 3       4  6       8  17     __________________________________________________________________________     POST-     EMERGENCE     Barley Igri 30      30 30      30 10     Barnyardgr. (Flood)                 25      20 25      35 20     Barnyardgrass                 20      50 25      95 10     Bedstraw    70      85 --      100                                       65     Blackgrass  20      25 40      40 0     Chickweed   40      60 45      95 45     Cocklebur   90      100                            90      75 50     Corn        20      20 25      50 10     Cotton      100     100                            100     100                                       100     Crabgrass   25      30 20      35 15     Downy Brome 15      15 20      0  0     Duck salad  0       0  0       0  30     Giant foxtail                 25      30 50      45 25     Italn. Rygrass                 0       0  0       35 0     Johnsongrass                 20      40 55      85 25     Lambsquarter                 40      65 90      100                                       60     Morningglory                 100     100                            100     100                                       70     Rape        80      90 100     100                                       95     Redroot Pigweed                 90      90 --      95 70     Rice Japonica                 20      20 15      45 30     Soybean     40      35 40      100                                       50     Speedwell   70      85 95      100                                       --     Sugar beet  100     95 100     100                                       100     Umbrella sedge                 0       0  0       0  20     Velvetleaf  100     100                            100     100                                       100     Watergrass  20      15 10      40 20     Wheat       20      0  10      35 0     Wild buckwheat                 90      100                            95      100                                       95     Wild oat    25      20 25      20 10     Rate 16 g/ha     __________________________________________________________________________     PREEMERGENCE     Barley Igri 0       0  0       0  0     Barnyardgrass                 20      0  10      50 0     Bedstraw    0       0  0       20 30     Blackgrass  0       0  0       10 0     Chickweed   0       0  10      50 0     Cocklebur   0       0  0       20 20     Corn        0       0  0       25 0     Cotton      0       0  0       90 100     Crabgrass   0       0  0       60 0     Downy Brome 0       0  0       0  0     Giant foxtail                 0       0  0       90 0     Italn. Rygrass                 0       0  0       0  0     Johnsongrass                 0       0  --      30 0     Lambsquarter                 10      0  95      100                                       15     Morningglory                 0       0  20      30 35     Rape        0       0  0       20 0     Redroot pigweed                 0       0  0       100                                       35     Soybean     0       0  0       30 20     Speedwell   0       0  25      100                                       0     Sugar beet  0       0  0       35 45     Velvetleaf  0       0  20      100                                       70     Wheat       0       0  0       0  0     Wild buckwheat                 0       0  0       85 85     Wild oat    0       0  0       10 0              COMPOUND             COMPOUND     Rate 8 g/ha              3  4  6  8  Rate 8 g/ha                                   3  4  6  8     __________________________________________________________________________     POST-                PREEMERGENCE     EMERGENCE     Barley Igri              30 20 30 30 Barley Igri                                   0  0  0  0     Barnyardgr. (Flood)              15 15 20 0  Barnyardgrass                                   0  0  10 40     Barnyardgrass              20 40 20 45 Bedstraw 0  0  0  15     Bedstraw 55 85 100                       70 Blackgrass                                   0  0  0  0     Blackgrass              20 25 35 20 Chickweed                                   0  0  10 30     Chickweed              40 60 30 70 Cocklebur                                   0  0  0  15     Cocklebur              80 90 90 65 Corn     0  0  0  0     Corn     15 15 20 30 Cotton   0  0  0  30     Cotton   100                 100                    100                       100                          Crabgrass                                   0  0  0  35     Crabgrass              25 20 20 20 Downy Brome                                   0  0  0  0     Downy Brome              10 0  10 0  Giant foxtail                                   0  0  0  35     Duck salad              0  0  0  0  Italn. Rygrass                                   0  0  0  0     Giant foxtail              25 25 35 30 Johnsongrass                                   0  0  0  10     Italn. Rygrass              0  0  0  10 Lambsquarter                                   0  0  20 100     Johnsongrass              20 -- 55 35 Morningglory                                   0  0  10 20     Lambsquarter              40 50 75 95 Rape     0  0  0  0     Morningglory              100                 100                    100                       90 Redroot Pigweed                                   0  0  0  90     Rape     80 30 100                       75 Soybean  0  0  0  0     Redroot Pigweed              90 80 90 95 Speedwell                                   0  -- 10 100     Rice Japonica              20 15 0  30 Sugar beet                                   0  0  0  --     Soybean  40 35 40 85 Velvetleaf                                   0  0  0  100     Speedwell              70 85 90 100                          Wheat    0  0  0  0     Sugar beet              100                 -- 100                       100                          Wild buckwheat                                   0  0  0  30     Umbrella sedge              0  0  0  0  Wild oat 0  0  0  0     Velvetleaf              100                 100                    100                       100     Watergrass              20 15 10 0     Wheat    10 0  10 30     Wild buckwheat              85 85 90 100     Wild oat 20 20 20 20     __________________________________________________________________________

Test C

Seeds of barnyardgrass (Echinochloa crus-galli), bindweed (Convolvulus arvensis), black nightshade (Solanum ptycanthum dunal), cassia (Cassia obtusifolia), cocklebur (Xanthium pensylvanicum), common ragweed (Ambrosia artemisiifolia), corn (Zea mays), cotton (Gossypium hirsutum), crabgrass (Digitaria spp.), fall panicum (Panicum dichotomiflorum), giant foxtail (Setaria faberii), green foxtail (Setaria viridis), jimsonweed (Datura stramonium), johnsongrass (Sorghum halepense), lambsquarter (Chenopodium album), morningglory (Ipomoea spp.), prickly sida (Sida spinosa), shattercane (Sorghum vulgare), signalgrass (Brachiaria platyphylla), smartweed (Polygonum pensylvanicum), soybean (Glycine max), sunflower (Helianthus annuus), velvetleaf (Abutilon theophrasti), wild proso (Panicum miliaceum), woolly cupgrass (Eriochloa villosa), yellow foxtail (Setaria lutescens) and purple nutsedge (Cyperus rotundus) tubers were planted into a matapeake sandy loam soil. These crops and weeds were grown in the greenhouse until the plants ranged in height from two to eighteen cm (one to four leaf stage), then treated postemergence with the test chemicals formulated in a non-phytotoxic solvent mixture which includes a surfactant. Pots receiving preemergence treatments were planted immediately prior to test chemical application. Pots treated in this fashion were placed in the greenhouse and maintained according to routine greenhouse procedures.

Treated plants and untreated controls were maintained in the greenhouse approximately 14-21 days after application of the test compound. Visual evaluations of plant injury responses were then recorded. Plant response ratings, summarized in Table C, are reported on a 0 to 100 scale where 0 is no effect and 100 is complete control.

    ______________________________________                 COM-                   COM-     TABLE C     POUND    TABLE C       POUND     ______________________________________     Rate 70 g/ha                 4        Rate 35 g/ha  4     POSTEMERGENCE        POSTEMERGENCE     Barnyardgrass                 95       Barnyardgrass 65     Bindweed    100      Bindweed      75     Blk Nightshade                 100      Blk Nightshade                                        85     Cassia      25       Cassia        20     Cocklebur   70       Cocklebur     50     Corn        35       Corn          25     Corn IR     35       Corn IR       30     Corn IT     35       Corn IT       30     Cotton      100      Cotton        100     Crabgrass   20       Crabgrass     0     Fall Panicum                 20       Fall Panicum  15     Giant Foxtail                 20       Giant Foxtail 15     Green Foxtail                 25       Green Foxtail 15     Jimsonweed  70       Jimsonweed    55     Johnson Grass                 25       Johnson Grass 15     Lambsquarter                 35       Lambsquarter  20     Morningglory                 100      Morningglory  100     Nutsedge    15       Nutsedge      0     Prickly Sida                 100      Prickly Sida  35     Ragweed     100      Ragweed       85     Shattercane 45       Shattercane   35     Signalgrass 15       Signalgrass   15     Smartweed   30       Smartweed     25     Soybean     45       Soybean       40     Soybean 4-4 55       Soybean 4-4   45     Soybean W20 45       Soybean W20   35     Sunflower   90       Sunflower     85     Velvetleaf  100      Velvetleaf    100     Wild Proso  30       Wild Proso    20     Woolly cupgrass                 30       Woolly cupgrass                                        25     Yellow Foxtail                 20       Yellow Foxtail                                        15     ______________________________________     Rate 17 g/ha                 4        Rate 8 g/ha    4  14     POSTEMERGENCE        POSTEMERGENCE     Barnyardgrass                 25       Barnyardgrass 10  15     Bindweed    45       Bindweed      25  --     Blk Nightshade                 65       Blk Nightshade                                        25  --     Cassia      15       Cassia        15  --     Cocklebur   35       Cocklebur     30  --     Corn        20       Corn          15  20     Corn IR     20       Corn IR       20  30     Corn IT     20       Corn IT       15  20     Cotton      75       Cotton        70  100     Crabgrass   0        Crabgrass      0  25     Fall Panicum                 10       Fall Panicum   0  15     Giant Foxtail                 10       Giant Foxtail 10  20     Green Foxtail                 15       Green Foxtail 10  25     Jimsonweed  30       Jimsonweed    25  --     Johnson Grass                 15       Johnson Grass 10  25     Lambsquarter                 15       Lambsquarter  10  --     Morningglory                 100      Morningglory  75  --     Nutsedge    0        Nutsedge       0  --     Prickly Sida                 30       Prickly Sida  25  --     Ragweed     60       Ragweed       25  --     Shattercane 30       Shattercane   25  25     Signalgrass 10       Signalgrass   0   --     Smartweed   20       Smartweed     15  --     Soybean     25       Soybean       20  45     Soybean 4--4                 35       Soybean 4--4  35  50     Soybean W20 30       Soybean W20   25  65     Sunflower   65       Sunflower     40  30     Velvetleaf  90       Velvetleaf    20  --     Wild Proso  15       Wild Proso    15  35     Woolly cupgrass                 15       Woolly cupgrass                                        15  30     Yellow Foxtail                 15       Yellow Foxtail                                        10  35     ______________________________________     Rate 4 g/ha  4    14     Rate 2 g/ha 14     POSTEMERGENCE            POSTEMERGENCE     Barnyardgrass                 10    10     Barnyardgrass                                           0     Bindweed    15    --     Bindweed    --     Blk Nightshade                 10    --     Blk Nightshade                                          --     Cassia      10    --     Cassia      --     Cocklebur   25    --     Cocklebur   --     Corn        10    15     Corn        10     Corn IR     10    20     Corn IR     10     Corn IT     15    10     Corn IT      0     Cotton      10    85     Cotton      75     Crabgrass    0    10     Crabgrass   10     Fall Panicum                  0    10     Fall Panicum                                           0     Giant Foxtail                  0    15     Giant Foxtail                                          10     Green Foxtail                 10    15     Green Foxtail                                           0     Jimsonweed  10    --     Jimsonweed  --     Johnson Grass                  0    20     Johnson Grass                                           0     Lambsquarter                  0    --     Lambsquarter                                          --     Morningglory                 25    --     Morningglory                                          --     Nutsedge     0    --     Nutsedge    --     Prickly Sida                 20    --     Prickly Sida                                          --     Ragweed     15    --     Ragweed     --     Shattercane 25    10     Shattercane  0     Signalgrass  0    --     Signalgrass --     Smartweed   10    --     Smartweed   --     Soybean     15    25     Soybean     10     Soybean 4-4 20    10     Soybean 4-4 10     Soybean W20 15    35     Soybean W20 10     Sunflower   10    25     Sunflower   15     Velvetleaf  10    --     Soybean     10     Wild Proso  10    25     Soybean 4-4 10     Woolly cupgrass                 10    15     Soybean W20 10     Yellow Foxtail                 10    25     Sunflower   15                              Velvetleaf  --                              Wild Proso  10                              Woolly cupgrass                                          10                              Yellow Foxtail                                          10     ______________________________________

Test D

Compounds evaluated in this test were formulated in a non-phytotoxic solvent mixture which includes a surfactant and applied to the soil surface before plant seedlings emerged (preemergence application) and to plants that were in the one-to-four leaf stage (postemergence application). A sandy loam soil was used for the preemergence test while a mixture of sandy loam soil and greenhouse potting mix in a 60:40 ratio was used for the postemergence test. Test compounds were applied within approximately one day after planting seeds for the preemergence test.

Plantings of these crops and weed species were adjusted to produce plants of appropriate size for the postemergence test. All plant species were grown using normal greenhouse practices. Crop and weed species include winter barley (Hordeum vulgare cv. `Igri`), blackgrass (Alopecurus myosuroides), chickweed (Stellaria media), downy brome (Bromus tectorum), galium (Galium aparine), green foxtail (Setaria viridis), kochia (Kochia scoparia), lambsquarters (Chenopodium album), speedwell (Veronica persica), rape (Brassica napus), ryegrass (Lolium multiflorum), sugar beet (Beta vulgaris cv. `US1`), spring wheat (Triticum aestivum cv. `ERA`), windgrass (Apera spica-venti), winter wheat (Triticum aestivum cv. `Talent`), wild buckwheat (Polygonum convolvulus), wild mustard (Sinapis arvensis), and wild oat (Avena fatua).

Treated plants and untreated controls were maintained in a greenhouse for approximately 21 to 28 days, after which all treated plants were compared to untreated controls and visually evaluated. Plant response ratings, summarized in Table D, are based upon a 0 to 100 scale where 0 is no effect and 100 is complete control. A dash response (-) means no test result.

                                      TABLE D     __________________________________________________________________________                COMPOUND           COMPOUND     __________________________________________________________________________     Rate 12 g/ha                8       Rate 8 g/ha                                   8     __________________________________________________________________________     POSTEMERGENCE      POSTEMERGENCE     Blackgrass 10      Blackgrass 10     Chickweed  75      Chickweed  55     Downy brome                10      Downy brome                                   10     Galium     100     Galium     100     Green foxtail                15      Green foxtail                                   40     Kochia     100     Kochia     100     Lambsquarters                95      Lambsquarters                                   80     Rape       100     Rape       100     Ryegrass   10      Ryegrass   10     Speedwell  100     speedwell  90     Sugar beet 100     Sugar beet 100     Wheat (Spring)                30      Wheat (Spring)                                   25     Wheat (Winter)                25      Wheat (Winter)                                   20     Wild buckwheat                100     Wild buckwheat                                   100     Wild mustard                100     Wild mustard                                   100     Wild oat   20      Wild oat   15     Windgrass  10      Windgrass  15     Winter Barley                20      Winter Barley                                   20     Rate 4 g/ha                8       Rate 2 g/ha                                   8     __________________________________________________________________________     POSTEMERGENCE      POSTEMERGENCE     Blackgrass 10      Blackgrass 5     Chickweed  50      Chickweed  15     Downy brome                5       Downy brome                                   o     Galium     70      Galium     50     Green foxtail                50      Green foxtail                                   30     Kochia     95      Kochia     40     Lambsquarters                70      Lambsquarters                                   50     Rape       85      Rape       --     Ryegrass   5       Ryegrass   5     Speedwell  65      Speedwell  55     Sugar beet 90      Sugar beet --     Wheat (Spring)                10      Wheat (Spring)                                   10     Wheat (Winter)                15      Wheat (Winter)                                   10     Wild buckwheat                85      Wild buckwheat                                   100     Wild mustard                100     Wild mustard                                   25     Wild oat   10      Wild oat   15     Windgrass  10      Windgrass  0     Winter Barley                15      Winter Barley                                   10     __________________________________________________________________________ 

We claim:
 1. A compound of Formula I, or an agriculturally-suitable salt thereof, ##STR44## wherein R¹ is H; F; Cl; or Br;R² is H; F; Cl; Br; CF₃ ; nitro; or cyano; R³ is H; C₁ -C₈ alkyl; C₃ C₈ cycloalkyl; C₃ -C₈ alkenyl; C₃ -C₈ alkynyl; C₁ -C₈ haloalkyl; C₂ -C₈ alkoxyalkyl; C₃ -C₈ alkoxyalkoxyalkyl; C₃ -C₈ haloalkynyl; C₃ -C₈ haloalkenyl; C₁ -C₈ alkylsulfonyl; C₁ -C₈ haloalkylsulfonyl; C₃ -C₈ alkoxycarbonylalkyl; S(O)₂ NH(C₁ -C₈ alkyl); C(O)R⁶ ; or benzyl optionally substituted on the phenyl ring with R⁷ ; R⁴ is H; C₁ -C₃ alkyl; or halogen; R⁵ is H; C₁ -C₆ alkyl; C₁ -C₆ haloalkyl; halogen; S(O)₂ (C₁ -C₆ alkyl); or C(═O)R⁸ ; or R⁴ and R⁵ are taken together along with the carbon to which they are attached to form a spiro-cyclopropane ring; R⁶ is C₁ -C₆ alkyl; C₁ -C₆ haloalkyl; C₁ -C₆ alkoxy; NH(C₁ C₆ alkyl); phenyl optionally substituted with R⁷ ; benzyl; or C₂ -C₈ dialkylamino; R⁷ is C₁ -C₆ alkyl; 1-2 halogen; C₁ -C₆ alkoxy; or CF₃ ; R⁸ is H; C₁ -C₆ alkyl; C₁ -C₆ alkoxy; or NH(C₁ -C₆ alkyl); J is ##STR45## wherein the dashed line in J-5, J-6 and J-12 indicates that the left-handed ring contains only single bonds or one bond in the ring is a carbon--carbon double bond; n and m are each independently 0; 1; 2; or 3; provided that m+n is 3; Z is CR⁹ R¹⁰ or N(C₁ -C₄ alkyl); each R⁹ is independently H; C₁ -C₃ alkyl; halogen; hydroxy; C₁ -C₆ alkoxy; C₁ -C₆ haloalkyl; C₁ -C₆ haloalkoxy; C₂ -C₆ alkylcarbonyloxy; or C₂ -C₆ haloalkylcarbonyloxy; each R¹⁰ is independently H; C₁ -C₃ alkyl; hydroxy; or halogen; R¹³ is H; C₁ -C₆ alkyl; C₁ -C₆ haloalkyl; C₃ -C₆ alkenyl; C₃ -C₆ haloalkenyl; C₃ -C₆ alkynyl; C₃ -C₆ haloalkynyl; HC(═O); (C₁ -C₄ alkyl) C(═O); or NH₂ ; R¹⁴ is C₁ -C₆ alkyl; C₁ -C₆ alkylthio; C₁ -C₆ haloalkyl; CF₃ ; or N(CH₃)₂ ; W is N or CR¹⁵ ; R¹⁵ is H; C₁ -C₆ alkyl; halogen; or phenyl optionally substituted with C₁ -C₆ alkyl, 1-2 halogen, C₁ -C₆ alkoxy, or CF₃ ; each Q is independently O or S; Q¹ is O or S; Z¹ is CR¹⁶ R¹⁷ or N(C₁ -C₄ alkyl); each R¹⁶ is independently H; halogen; hydroxy; C₁ -C₆ alkoxy; C₁ -C₆ haloalkyl; C₁ -C₆ haloalkoxy; C₂ -C₆ alkylcarbonyloxy; or C₂ -C₆ haloalkylcarbonyloxy; each R¹⁷ is independently H; hydroxy; or halogen; or when R¹⁶ and R¹⁷ are bonded to adjacent atoms they can be taken together with the carbons to which they are attached to form ##STR46## R¹⁸ is C₁ -C₆ alkyl; halogen; or C₁ -C₆ haloalkyl; R¹⁹ and R²⁰ are each independently H; C₁ -C₆ alkyl; or C₁ -C₆ haloalkyl; R²³ is halogen or cyano; and R²⁶ is C₁ -C₆ alkyl; C₁ -C₆ haloalkyl; or phenyl optionally substituted with C₁ -C₆ alkyl, 1-2 halogen, 1-2 nitro, C₁ -C₆ alkoxy, or CF₃.
 2. A compound of claim 1 wherein:R¹ is F or Cl; R² is F; Cl; or Br; R³ is H; C₁ -C₆ alkyl; C₃ -C₆ cycloalkyl; C₃ -C₆ alkynyl; C₁ -C₆ haloalkyl; C₂ -C₆ alkoxyalkyl; C₃ -C₆ alkenyl; C₃ -C₆ haloalkenyl; C₁ -C₆ alkylsufonyl; C₃ -C₆ alkoxycarbonylalkyl; C(O)R⁶ ; or benzyl optionally substituted on the phenyl ring with R⁷ ; R⁴ is H or halogen; R⁵ is H; J is J-1; J-2; J-4; J-5; J-6; J-12; or J-15; Z is CR⁹ R¹⁰ or N(C₁ -C₄ alkyl); each R⁹ is independently H; halogen; or C₁ -C₆ haloalkoxy; each R¹⁰ is independently H or halogen; each Q is O; Q¹ is S; Z¹ is CR₁₆ R¹⁷ or N(C₁ -C₄ alkyl); each R¹⁶ is independently H; halogen; or haloalkoxy; each R¹⁷ is independently H or halogen; or when R¹⁶ and R¹⁷ are bonded to adjacent atoms they can be taken together with the carbons to which they are attached to form ##STR47## R¹⁸ is t-butyl or CH₂ CH₂ CH₂ F; and R²³ is Cl or cyano.
 3. A compound of claim 2 wherein:R² is F or Cl; R³ is C₁ -C₆ alkyl; C₃ -C₆ cycloalkyl; C₃ -C₆ alkenyl; C₃ -C₆ alkynyl; C₃ -C₆ alkoxycarbonylalkyl; or benzyl optionally substituted on the phenyl ring with R⁷ ; J is J-1; J-2; J-4; J-5; J-6; or J-12; Z is CR⁹ R¹⁰ ; each R⁹ is independently H or halogen; R¹³ is CH₃ ; R¹⁴ is CF₃ ; W is CH; Z¹ is CR¹⁶ R¹⁷ ; each R¹⁶ is independently H or halogen; each R¹⁷ is independently H or halogen; or when R¹⁶ and R¹⁷ are bonded to adjacent atoms they can be taken together with the carbons to which they are attached to from ##STR48##
 4. A compound of claim 3 wherein:R² is Cl; R³ is C₁ -C₆ alkyl; C₃ -C₆ alkenyl; or C₃ -C₆ alkynyl; J is J-1; J-2; J-4; J-6; J-12; Z is CR⁹ R¹⁰ ; R⁹ is independently H or F; R¹⁰ is independently H or F; Z¹ is CR¹⁶ R¹⁷ ; R¹⁶ is independently H or F; and R¹⁷ is independently H or F.
 5. A compound of claim 1 of Formula I.
 6. A compound of claim 2 which is selected from the group:3- 7-chloro-5-fluoro-1,3-dihydro-1- (4-methoxyphenyl)methyl!-2,1-benzisothiazol-4-yl!-1-methyl-6-tritluoromethyl)-2,4(1H, 3H)-pyrimidinedione S,S-dioxide; 3-(7-chloro-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-yl)-1-methyl-6-(trifluoromethyl)-2,4(1H, 3H)-pyrimidinedione S,S-dioxide; 3-(7-chloro-1-ethyl-5-fluoro-1,3-dihydro-2,1 benzisothiazol-4-yl)-1-methyl-6-(trifluoromethyl)-2,4(1H, 3H)-pyrimidinedione S,S-dioxide; and 3- (7-chloro-1-ethyl-5-fluoro-1,3-dihydro-2,1-benzisothiazol-4-yl) imino!tetrahydro-1H, 3H 1,3,4!thiodiazol 3,4-a!pyridazin-1-one S,S-dioxide.
 7. A herbicidal composition comprising an effective amount of a compound according to claim 1 and at least one of a surfactant, a solid diluent or a liquid diluent.
 8. A herbicidal composition comprising an effective amount of a compound according to claim 2 and at least one of a surfactant, a solid diluent or a liquid diluent.
 9. A method for controlling the growth of undesired vegetation comprising contacting the vegetation or its enviroment with a herbicidally effective amount of a composition of claim
 7. 